Extracellular Matrix Compositions

ABSTRACT

The present invention is directed to a method of producing compositions including embryonic proteins. The method includes culturing cells under hypoxic conditions on a biocompatible three-dimensional surface in vitro. The culturing method produces both soluble and non-soluble fractions, which may be used separately or in combination to obtain physiologically acceptable compositions useful in a variety of medical and therapeutic applications.

CROSS REFERENCE TO RELATED APPLICATION(S)

This application claims the benefit of priority under 35 U.S.C. §119(e)of U.S. Ser. No. 61/024,854, filed Jan. 30, 2008; the benefit ofpriority under 35 U.S.C. §119(e) of U.S. Application Ser. No.61/034,361, filed Mar. 6, 2008; and the benefit of priority under 35U.S.C. §119(e) of U.S. Application Ser. No. 61/050,940, filed May 6,2008. The disclosure of each of the prior applications is consideredpart of and is incorporated by reference in the disclosure of thisapplication.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to the production and use ofextracellular matrix compositions and more specifically to proteinsobtained by culturing cells under hypoxic conditions on a surface in asuitable growth medium.

2. Background Information

The extracellular matrix (ECM) is a complex structural entitysurrounding and supporting cells that are found in vivo within mammaliantissues. The ECM is often referred to as the connective tissue. The ECMis primarily composed of three major classes of biomolecules includingstructural proteins such as collagens and elastins, specialized proteinssuch as fibrillins, fibronectins, and laminins, and proteoglycans.

Growth of ECM compositions in vitro and their use in a variety oftherapeutic and medical applications have been described in the art. Onetherapeutic application of such ECM compositions includes treatment andrepair of soft tissue and skin defects such as wrinkles and scars.

The repair or augmentation of soft tissue defects caused by defects,such as, acne, surgical scarring or aging has proven to be verydifficult. A number of materials have been used to correct soft tissuedefects with varying degrees of success, however, no material has beencompletely safe and effective. For example, silicon causes a variety ofphysiological and clinical problems including long term side effects,such as nodules, recurring cellulitis and skin ulcers.

Collagen compositions have also been used as an injectable material forsoft tissue augmentation. Collagen is the main protein of connectivetissue and the most abundant protein in mammals, making up about 25% ofthe total protein content. There are currently 28 types of collagendescribed in literature (see, e.g., Tables 1 and 2 infra, for a detailedlisting). However, over 90% of the collagen in the body are Collagens I,II, III, and IV.

Different collagen materials have been used for treatment of soft tissuedefects, such as reconstituted injectable bovine collagen, crosslinkedcollagen, or other xenogeneic collagens. However, several problems existwith such collagens. A common problem includes the complexity and highcost of producing the implant materials to remove potentiallyimmunogenic substances to avoid allergic reactions in the subject.Additionally, treatments using such collagens have not proven longlasting.

Other materials have also been described that may be used for softtissue repair or augmentation, such as, biocompatible ceramic particlesin aqueous gels (U.S. Pat. No. 5,204,382), thermoplastic and/orthermosetting materials (U.S. Pat. No. 5,278,202), and lactic acid basedpolymer blends (U.S. Pat. No. 4,235,312). Additionally, use of naturallysecreted ECM compositions have also been described (U.S. Pat. No.6,284,284). However, such materials have all proven to have limitations.

Accordingly, new materials are needed for soft tissue repair andaugmentation that overcome the deficiencies of prior materials. The needexists to provide a safe, injectable, long lasting, bioabsorbable, softtissue repair and augmentation material.

In vitro cultured ECM compositions can additionally be used to treatdamaged tissue, such as, damaged cardiac muscle and related tissue. Thecompositions are useful as implants or biological coatings onimplantable devices, such as, stents; vascular prosthesis to promotevascularization in organs, such as the heart and related tissue; anddevices useful in hernia repair, pelvic floor repair, wound repair, androtator cuff repair, such as patches and the like.

Coronary heart disease (CHD), also called coronary artery disease (CAD),ischaemic heart disease, and atherosclerotic heart disease, ischaracterized by a narrowing of the small blood vessels that supplyblood and oxygen to the heart. Coronary heart disease is usually causedby a condition called atherosclerosis, which occurs when fatty materialand plaque builds up on the walls of arteries causing the arteries tonarrow. As the coronary arteries narrow, blood flow to the heart canslow down or stop, causing chest pain (stable angina), shortness ofbreath, heart attack, and other symptoms.

Coronary heart disease (CHD) is the leading cause of death in the UnitedStates for men and women. According to the American Heart Association,more than 15 million people have some form of the condition. While thesymptoms and signs of coronary heart disease are evident in the advancedstate of the disease, most individuals with coronary heart disease showno evidence of disease for decades as the disease progresses before asudden heart attack occurs. The disease is the most common cause ofsudden death, and is also the most common reason for death of men andwomen over 20 years of age. According to present trends in the UnitedStates, half of healthy 40-year-old males will develop CHD in thefuture, as well as one in three healthy 40-year-old women.

Current methods for improving blood flow in a diseased or otherwisedamaged heart involve invasive surgical techniques, such as, coronaryby-pass surgery, angioplasty, and endarterectomy. Such proceduresnaturally involve high-degrees of inherent risk during and aftersurgery, and often only provide a temporary remedy to cardiac ischemia.Accordingly, new treatment options are required to increase the successof currently available techniques for treating CHD and related symptoms.

In vitro cultured ECM compositions can additionally be used to repairand/or regenerate damaged cells or tissue, such as chondral orosteochondral cells. Osteochondral tissue is any tissue that relates toor contains bone or cartilage. The compositions of the present inventionare useful for treatment of osteochondral defects, such as degenerativeconnective tissue diseases, such as rheumatoid and/or osteoarthritis aswell as defects in patients who have cartilage defects due to trauma.

Current attempts at repairing osteochondral defects include implantationof human chondrocytes in biocompatible and biodegradable hydrogel graftsin attempts to improve the possibilities to restore articular cartilagelesions. Additionally, the technique of chondrocyte culture in alginatebeads or a matrix including polysulphated alginate has been described togenerate a hyaline-like cartilagineous tissue. However, attempts atrepairing enchondral lesions of articular cartilage by implantation ofhuman autologous chondrocytes have had limited success. Accordingly, newtreatment options are required to increase the success of currentlyavailable techniques for treating ostechondral defects.

In vitro cultured ECM compositions are also useful in tissue culturesystems for generation of engineered tissue implants. The field oftissue engineering involves the use of cell culture technology togenerate new biological tissues or repair damaged tissues. Fueled inpart, by the stem cell revolution, tissue engineering technology offersthe promise of tissue regeneration and replacement following trauma ortreatment of degenerative diseases. It can also be used in the contextof cosmetic procedures.

Tissue engineering techniques can be used to generate both autologousand heterologous tissue or cells using a variety of cell types andculture techniques. In creating an autologous implant, donor tissue maybe harvested and dissociated into individual cells, and subsequentlyattached and cultured on a substrate to be implanted at the desired siteof the functioning tissue. Many isolated cell types can be expanded invitro using cell culture techniques, however, anchorage dependent cellsrequire specific environments, often including the presence of athree-dimensional scaffold, to act as a template for growth.

Current tissue engineering technology provide generally, artificialimplants. Successful cell transplantation therapy depends on thedevelopment of suitable substrates for both in vitro and in vivo tissueculture. Thus the development of an ECM that contains only naturalmaterials and that is suitable for implantation would have more of thecharacteristics of the endogenous tissue. Accordingly, generation ofnatural ECM material is an ongoing challenge in the field of tissueengineering.

SUMMARY OF THE INVENTION

The present invention is based in part on the seminal discovery thatcells cultured on surfaces (e.g., two-dimensional or three-dimensional)under conditions that stimulate the early embryonic environment (e.g.,hypoxia and reduced gravitational forces) produce ECM compositions withfetal properties. The ECM compositions produced by culturing cells underhypoxic conditions on a surface containing one or more embryonicproteins have a variety of beneficial applications.

In one embodiment, the present invention provides a method of making ECMcompositions containing one or more embryonic proteins. The methodincludes culturing cells under hypoxic conditions on a surface (e.g.,two-dimensional or three-dimensional) in a suitable growth medium toproduce a soluble and non-soluble fraction. In various aspects, thecompositions include the soluble or non-soluble fraction separately, aswell as combinations of the soluble and insoluble fraction. In variousaspects, the compositions produced include upregulation of geneexpression and production of laminins, collagens and Wnt factors. Inother aspects the compositions produced include downregulation of geneexpression of laminins, collagens and Wnt factors. In other aspects, thecompositions are species specific and include cells and/or biologicalmaterial from a single animal species. While in vitro cultured ECMcompositions are useful in the treatment of humans, such compositionsmay be applied to other species of animals. Accordingly, suchcompositions are well suited for veterinary applications.

In another embodiment, the present invention provides a method ofproducing a Wnt protein and a vascular endothelial growth factor (VEGF).The method includes culturing cells under hypoxic conditions on asurface (e.g., two-dimensional or three-dimensional) in a suitablegrowth medium, thereby producing the Wnt protein and the VEGF. Invarious aspects, the growth medium is serum-free and the hypoxic oxygenconditions are 1-5% oxygen. In related aspects, the Wnt species areupregulated as compared with media produced in oxygen conditions ofabout 15-20% oxygen. In an exemplary aspect, the Wnt species are wnt 7aand wnt 11.

In another embodiment, the present invention includes a method of repairand/or regeneration of cells by contacting cells to be repaired orregenerated with the ECM compositions described herein. In one aspect,the cells are osteochondral cells. Accordingly, the method contemplatesrepair of osteochondral defects.

In another embodiment, ECM compositions are useful as implants orbiological coatings on implantable devices. In various aspects, thecompositions of the present invention are included in implants orutilized as biological coatings on implantable devices, such as, stents;and vascular prosthesis to promote vascularization in organs, such asthe heart and related tissue. In a related aspect, the compositions areincluded in tissue regeneration patches or implants, useful in herniarepair, pelvic floor repair, wound repair, rotator cuff repair, and thelike.

In yet another embodiment the present invention includes a method forimprovement of a skin surface in a subject including administering tothe subject at the site of a wrinkle, the ECM compositions describedherein. In yet a further embodiment, the present invention includes amethod for soft tissue repair or augmentation in a subject includingadministering to the subject at the site of a wrinkle, the ECMcompositions described herein.

In another embodiment, the present invention includes a tissue culturesystem. In various aspects, the culture system is composed of the ECMcompositions described herein, such as being included in two-dimensionalor three-dimensional support materials. In another aspect, the ECMcompositions described herein serve as a support or two-dimensional orthree-dimensional support for the growth of various cell types. Forexample, the culture system can be used to support the growth of stemcells. In one aspect, the stem cells are embryonic stem cells,mesenchymal stem cells or neuronal stem cells.

In another embodiment, the compositions of the present invention can beused to provide a surface coating used in association with implantationof a device in a subject to promote endothelialization andvascularization.

In another embodiment, the compositions of the present invention can beused to provide a method of treating damaged tissue. The method includescontacting the damaged tissue with a composition generated by culturingcells under hypoxic conditions on a two-dimensional or three-dimensionalsurface containing one or more embryonic proteins under conditions thatallow for treatment of the damaged tissue.

In another embodiment, the present invention includes a biologicalvehicle for cell delivery or maintenance at a site of delivery includingthe ECM compositions described herein. The vehicle can be used in suchapplications as injections of cells, such as stem cells, into damagedheart muscle or for tendon and ligament repair.

In another embodiment, the present invention provides a method forstimulating or promoting hair growth. The method includes contacting acell with the ECM compositions described herein. In an exemplary aspect,the cell is a hair follicle cell. In various aspects the cell may becontacted in vivo or ex vivo.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows graphical representations of FBGC formation 2 weeks afterimplantation of polypropylene mesh coated with hECM. FIG. 1A shows thenumber of FBGCs per fiber 2 weeks after implantation for uncoated (firstcolumn) and hECM coated fibers (second column). FIG. 1B shows the numberof FBGCs per fiber 2 weeks after implantation for uncoated (columns 1-3)and ECM coated fibers (columns 4-6). * indicates p<0.05.

FIG. 2 shows graphical representations of FBGC formation 2 weeks afterimplantation of polypropylene mesh coated with hECM. FIG. 2A shows thenumber of FBGCs per fiber 5 weeks after implantation for uncoated (firstcolumn) and hECM coated fibers (second column). FIG. 2B shows the numberof FBGCs per fiber 5 weeks after implantation for uncoated (columns 1and 3) and hECM coated fibers (columns 2 and 4).

FIG. 3 shows pictorial representations of human hair follicle cells.FIG. 3A is an image of human hair follicle cells after cell culture forfour weeks in the presence of hECM and subsequent transplantation into amouse and growth for 4 additional weeks, while FIG. 3B is an image ofcontrol follicle cells.

FIG. 4 shows a graphical representation of fibroblastic metabolicresponse to extracellular matrix compositions (both mouse ECM and humanECM) as shown by MTT assay.

FIG. 5 is a graphical representation of cell number in response to humanfibroblast exposure to hECM as measured by the Pico Green Assay.

FIG. 6 is a graphical representation of erythema evaluations for 41human subjects taken at 3, 7 and 14 days post laser treatment. Theseverity of erythema was evaluated on a scale of 0 (none) to 4 (severe).Each group of 4 data sets (0.1×hECM, 1×hECM, 10×hECM, and control fromleft to right) represents evaluations at day 3 (left), 7 (middle) and 14(right).

FIG. 7 is a graphical representation of edema evaluations for 41 humansubjects taken at 3, 7 and 14 days post laser treatment. The severity oferythema was evaluated on a scale of 0 (none) to 2.5 (severe). Eachgroup of 4 data sets (0.1×hECM, 1×hECM, 10×hECM, and control from leftto right) represents evaluations at day 3 (left), 7 (middle) and 14(right).

FIG. 8 is a graphical representation of crusting evaluations for 41human subjects taken at 3, 7 and 14 days post laser treatment. Theseverity of erythema was evaluated on a scale of 0 (none) to 3.5(severe). Each group of 4 data sets (0.1×hECM, 1×hECM, 10×hECM, andcontrol from left to right) represents evaluations at day 3 (left), 7(middle) and 14 (right).

FIG. 9 is a graphical representation of transepidermal water loss (TWEL)values for 41 human subjects taken at 3, 7 and 14 days post lasertreatment. The severity of TWEL was evaluated on a scale of 0 (none) to4 (severe). Each group of 4 data sets (0.1×hECM, 1×hECM, 10×hECM, andcontrol from left to right) represents evaluations at day 3 (left), 7(middle) and 14 (right).

FIG. 10 is a graphical representation of three dimensional profilometryimage analysis of silicon replicas from the peri-ocular area. Datapoints were taken for 22 subjects before laser treatment, 4 weeks posttreatment, and 10 weeks post treatment. Data series A represents valuesfor hECM administration; data series B represents the control.

FIG. 11 is a graphical representation of analysis of petrolatum use postlaser surgery.

FIG. 12 is a graphical representation of analysis of skin erythema withdata points taken at days 0, 3, 5, 7, 10 and 14 post laser surgery.

FIG. 13 is a graphical representation of mexameter analysis with datapoints taken at days 0, 3, 5, 7, 10 and 14 post laser surgery.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a method for making ECM compositionsthat include one or more embryonic proteins. In particular thecompositions are generated by culturing cells under hypoxic conditionson a surface (e.g., two-dimensional or three-dimensional) in a suitablegrowth medium. The culturing method produces both soluble andnon-soluble fractions which may be used separately or in combination toobtain physiologically acceptable compositions having a variety ofapplications.

The compositions of the present invention have a variety of applicationsincluding, but not limited to, promoting repair and/or regeneration ofdamaged cells or tissues, use in patches and implants to promote tissueregeneration (e.g., hernial repair, pelvic floor repair, rotator cuffrepair, and wound repair), use in tissue culture systems for culturingcells, such as stem cells, use in surface coatings used in associationwith implantable devices (e.g., pacemakers, stents, stent grafts,vascular prostheses, heart valves, shunts, drug delivery ports orcatheters, hernial and pelvic floor repair patches), promoting softtissue repair, augmentation, and/or improvement of a skin surface, suchas wrinkles, use as a biological anti-adhesion agent or as a biologicalvehicle for cell delivery or maintenance at a site of delivery.

The invention is based in part, on the discovery that cells cultured onthree-dimensional surfaces under conditions that stimulate the earlyembryonic environment (hypoxia and reduced gravitational forces) priorto angiogenesis produces ECM compositions with fetal properties,including generation of embryonic proteins. Growth of cells underhypoxic conditions demonstrate a unique ECM with fetal properties andgrowth factor expression. Unlike the culturing of ECM under traditionalculture conditions, over 5000 genes are differentially expressed in ECMcultured under hypoxic conditions. This results in a cultured ECM thathas different properties and a different biological composition. Forexample, an ECM produced under hypoxic conditions is similar to fetalmesenchymal tissue in that it is relatively rich in collagens type III,IV, and V, and glycoproteins such as fibronectin, SPARC, thrombospondin,and hyaluronic acid.

Hypoxia also enhances expression of factors which regulate wound healingand organogenesis, such as VEGF, FGF-7, and TGF-β, as well as multipleWnt factors including writs 2b, 4, 7a, 10a, and 11. Cultured embryonichuman ECM also stimulates an increase of metabolic activity in humanfibroblasts in vitro, as measured by increased enzymatic activity.Additionally, there is an increase in cell number in response to thecultured embryonic ECM.

Before the present compositions and methods are described, it is to beunderstood that this invention is not limited to particularcompositions, methods, and experimental conditions described, as suchcompositions, methods, and conditions may vary. It is also to beunderstood that the terminology used herein is for purposes ofdescribing particular embodiments only, and is not intended to belimiting, since the scope of the present invention will be limited onlyin the appended claims.

As used in this specification and the appended claims, the singularforms “a”, “an”, and “the” include plural references unless the contextclearly dictates otherwise. Thus, for example, references to “themethod” includes one or more methods, and/or steps of the type describedherein which will become apparent to those persons skilled in the artupon reading this disclosure and so forth.

In various embodiments, the present invention involves methods formaking ECM compositions that include one or more embryonic proteins andapplications thereof. In particular the compositions are generated byculturing cells under hypoxic conditions on a two-dimensional orthree-dimensional surface in a suitable growth medium. The compositionsare derived by growing cells on a three-dimensional framework resultingin a multi-layer cell culture system. Cells grown on a three-dimensionalframework support, in accordance with the present invention, grow inmultiple layers, forming a cellular matrix. Growth of the cultured cellsunder hypoxic conditions results in differential gene expression as theresult of hypoxic culturing conditions versus traditional culture.

ECM is a composition of proteins and biopolymers that substantiallycomprise tissue that is produced by cultivation of cells. Stromal cells,such as fibroblasts, are an anchorage dependant cell type requiringgrowth while attached to materials and surfaces suitable for cellculture. The ECM materials produced by the cultured cells are depositedin a three-dimensional arrangement providing spaces for the formation oftissue-like structures.

The cultivation materials providing three-dimensional architectures arereferred to as scaffolds. Spaces for deposition of ECM are in the formof openings within, for example woven mesh or interstitial spacescreated in a compacted configuration of spherical beads, calledmicrocarriers.

As used herein, “extracellular matrix composition” includes both solubleand non-soluble fractions or any portion thereof. The non-solublefraction includes those secreted ECM proteins and biological componentsthat are deposited on the support or scaffold. The soluble fractionincludes refers to culture media in which cells have been cultured andinto which the cells have secreted active agent(s) and includes thoseproteins and biological components not deposited on the scaffold. Bothfractions may be collected, and optionally further processed, and usedindividually or in combination in a variety of applications as describedherein.

The three-dimensional support or scaffold used to culture stromal cellsmay be of any material and/or shape that: (a) allows cells to attach toit (or can be modified to allow cells to attach to it); and (b) allowscells to grow in more than one layer (i.e., form a three dimensionaltissue). In other embodiments, a substantially two-dimensional sheet ormembrane or beads may be used to culture cells that are sufficientlythree dimensional in form.

The biocompatible material is formed into a three-dimensional structureor scaffold, where the structure has interstitial spaces for attachmentand growth of cells into a three dimensional tissue. The openings and/orinterstitial spaces of the framework in some embodiments are of anappropriate size to allow the cells to stretch across the openings orspaces. Maintaining actively growing cells stretched across theframework appears to enhance production of the repertoire of growthfactors responsible for the activities described herein. If the openingsare too small, the cells may rapidly achieve confluence but be unable toeasily exit from the mesh. These trapped cells may exhibit contactinhibition and cease production of the appropriate factors necessary tosupport proliferation and maintain long term cultures. If the openingsare too large, the cells may be unable to stretch across the opening,which may lead to a decrease in stromal cell production of theappropriate factors necessary to support proliferation and maintain longterm cultures. Typically, the interstitial spaces are at least about 100um, at least 140 um, at least about 150 um, at least about 180 um, atleast about 200 um, or at least about 220 um. When using a mesh type ofmatrix, as exemplified herein, we have found that openings ranging fromabout 100 μm to about 220 μm will work satisfactorily. However,depending upon the three-dimensional structure and intricacy of theframework, other sizes are permissible. Any shape or structure thatallows the cells to stretch and continue to replicate and grow forlengthy time periods may function to elaborate the cellular factors inaccordance with the methods herein.

In some aspects, the three dimensional framework is formed from polymersor threads that are braided, woven, knitted or otherwise arranged toform a framework, such as a mesh or fabric. The materials may also beformed by casting of the material or fabrication into a foam, matrix, orsponge-like scaffold. In other aspects, the three dimensional frameworkis in the form of matted fibers made by pressing polymers or otherfibers together to generate a material with interstitial spaces. Thethree dimensional framework may take any form or geometry for the growthof cells in culture. Thus, other forms of the framework, as furtherdescribed below, may suffice for generating the appropriate conditionedmedium.

A number of different materials may be used to form the scaffold orframework. These materials include non-polymeric and polymericmaterials. Polymers, when used, may be any type of polymer, such ashomopolymers, random polymers, copolymers, block polymers, coblockpolymers (e.g., di, tri, etc.), linear or branched polymers, andcrosslinked or non-crosslinked polymers. Non-limiting examples ofmaterials for use as scaffolds or frameworks include, among others,glass fibers, polyethylenes, polypropylenes, polyamides (e.g., nylon),polyesters (e.g., dacron), polystyrenes, polyacrylates, polyvinylcompounds (e.g., polyvinylchloride; PVC), polycarbonates,polytetrafluorethylenes (PTFE; TEFLON), thermanox (TPX), nitrocellulose,polysaacharides (e.g., celluloses, chitosan, agarose), polypeptides(e.g., silk, gelatin, collagen), polyglycolic acid (PGA), and dextran.

In some aspects, the framework or beads may be made of materials thatdegrade over time under the conditions of use. Biodegradable also refersto absorbability or degradation of a compound or composition whenadministered in vivo or under in vitro conditions. Biodegradation mayoccur through the action of biological agents, either directly orindirectly. Non-limiting examples of biodegradable materials include,among others, polylactide, polyglycolide, poly(trimethylene carbonate),poly(lactide-co-glycolide) (i.e., PLGA), polyethylene terephtalate(PET), polycaprolactone, catgut suture material, collagen (e.g., equinecollagen foam), polylactic acid, or hyaluronic acid. For example, thesematerials may be woven into a three-dimensional framework such as acollagen sponge or collagen gel.

In other aspects, where the cultures are to be maintained for longperiods of time, cryopreserved, and/or where additional structuralintegrity is desired, the three dimensional framework may be comprisedof a nonbiodegradable material. As used herein, a nonbiodegradablematerial refers to a material that does not degrade or decomposesignificantly under the conditions in the culture medium. Exemplarynondegradable materials include, as non-limiting examples, nylon,dacron, polystyrene, polyacrylates, polyvinyls, polytetrafluoroethylenes(PTFE), expanded PTFE (ePTFE), and cellulose. An exemplary nondegradingthree dimensional framework comprises a nylon mesh, available under thetradename Nitex®, a nylon filtration mesh having an average pore size of140 μm and an average nylon fiber diameter of 90 μm (#3-210/36, Tetko,Inc., N.Y.).

In other aspects, the beads, scaffold or framework is a combination ofbiodegradeable and non-biodegradeable materials. The non-biodegradablematerial provides stability to the three dimensional scaffold duringculturing while the biodegradeable material allows formation ofinterstitial spaces sufficient for generating cell networks that producethe cellular factors sufficient for therapeutic applications. Thebiodegradable material may be coated onto the non-biodegradable materialor woven, braided or formed into a mesh. Various combinations ofbiodegradable and non-biodegradable materials may be used. An exemplarycombination is poly(ethylene therephtalate) (PET) fabrics coated with athin biodegradable polymer film, poly[D-L-lactic-co-glycolic acid), inorder to obtain a polar structure.

In various aspects, the scaffold or framework material may bepre-treated prior to inoculation with cells to enhance cell attachment.For example, prior to inoculation with cells, nylon screens in someembodiments are treated with 0.1 M acetic acid, and incubated inpolylysine, fetal bovine serum, and/or collagen to coat the nylon.Polystyrene could be similarly treated using sulfuric acid. In otherembodiments, the growth of cells in the presence of thethree-dimensional support framework may be further enhanced by adding tothe framework or coating it with proteins (e.g., collagens, elastinfibers, reticular fibers), glycoproteins, glycosaminoglycans (e.g.,heparan sulfate, chondroitin-4-sulfate, chondroitin-6-sulfate, dermatansulfate, keratan sulfate, etc.), fibronectins, and/or glycopolymer(poly[N-p-vinylbenzyl-D-lactoamide], PVLA) in order to improve cellattachment. Treatment of the scaffold or framework is useful where thematerial is a poor substrate for the attachment of cells.

In one aspect, mesh is used for production of ECM. The mesh is a wovennylon 6 material in a plain weave form with approximately 100 μmopenings and approximately 125 μm thick. In culture, fibroblast cellsattach to the nylon through charged protein interactions and grow intothe voids of the mesh while producing and depositing ECM proteins. Meshopenings that are excessively large or small may not be effective butcould differ from those above without substantially altering the abilityto produce or deposit ECM. In another aspect, other woven materials areused for ECM production, such as polyolefin's, in weave configurationsgiving adequate geometry for cell growth and ECM deposition.

For example, nylon mesh is prepared for cultivation in any of the stepsof the invention by cutting to the desired size, washing with 0.1-0.5Macetic acid followed by rinsing with high purity water and then steamsterilized. For use as a three-dimensional scaffold for ECM productionthe mesh is sized into squares approximately 10 cm×10 cm. However, themesh could be any size appropriate to the intended application and maybe used in any of the methods of the present invention, includingcultivation methods for inoculation, cell growth and ECM production andpreparation of the final form.

In other aspects, the scaffold for generating the cultured tissues iscomposed of microcarriers, which are beads or particles. The beads maybe microscopic or macroscopic and may further be dimensioned so as topermit penetration into tissues or compacted to form a particulargeometry. In some tissue penetrating embodiments, the framework for thecell cultures comprises particles that, in combination with the cells,form a three dimensional tissue. The cells attach to the particles andto each other to form a three dimensional tissue. The complex of theparticles and cells is of sufficient size to be administered intotissues or organs, such as by injection or catheter. Beads ormicrocarriers are typically considered a two-dimensional system orscaffold.

As used herein, a “microcarriers” refers to a particle having size ofnanometers to micrometers, where the particles may be any shape orgeometry, being irregular, non-spherical, spherical, or ellipsoid.

The size of the microcarriers suitable for the purposes herein can be ofany size suitable for the particular application. In some embodiments,the size of microcarriers suitable for the three dimensional tissues maybe those administrable by injection. In some embodiments, themicrocarriers have a particle size range of at least about 1 μm, atleast about 10 μm, at least about 25 μm, at least about 50 μm, at leastabout 100 μm, at least about 200 μm, at least about 300 μm, at leastabout 400 μm, at least about 500 μm, at least about 600 μm, at leastabout 700 μm, at least about 800 μm, at least about 900 μm, at leastabout 1000 μm.

In some aspects in which the microcarriers are made of biodegradablematerials. In some aspects, microcarriers comprising two or more layersof different biodegradable polymers may be used. In some embodiments, atleast an outer first layer has biodegradable properties for forming thethree dimensional tissues in culture, while at least a biodegradableinner second layer, with properties different from the first layer, ismade to erode when administered into a tissue or organ.

In some aspects, the microcarriers are porous microcarriers. Porousmicrocarriers refer to microcarriers having interstices through whichmolecules may diffuse in or out from the microparticle. In otherembodiments, the microcarriers are non-porous microcarriers. A nonporousmicroparticle refers to a microparticle in which molecules of a selectsize do not diffuse in or out of the microparticle.

Microcarriers for use in the compositions are biocompatible and have lowor no toxicity to cells. Suitable microcarriers may be chosen dependingon the tissue to be treated, type of damage to be treated, the length oftreatment desired, longevity of the cell culture in vivo, and timerequired to form the three dimensional tissues. The microcarriers maycomprise various polymers, natural or synthetic, charged (i.e., anionicor cationic) or uncharged, biodegradable, or nonbiodegradable. Thepolymers may be homopolymers, random copolymers, block copolymers, graftcopolymers, and branched polymers.

In some aspects, the microcarriers comprise non-biodegradablemicrocarriers. Non-biodegradable microcapsules and microcarriersinclude, but not limited to, those made of polysulfones,poly(acrylonitrile-co-vinyl chloride), ethylene-vinyl acetate,hydroxyethylmethacrylate-methyl-methacrylate copolymers. These areuseful to provide tissue bulking properties or in embodiments where themicrocarriers are eliminated by the body.

In some aspects, the microcarriers comprise degradable scaffolds. Theseinclude microcarriers made from naturally occurring polymers,non-limiting example of which include, among others, fibrin, casein,serum albumin, collagen, gelatin, lecithin, chitosan, alginate orpoly-amino acids such as poly-lysine. In other aspects, the degradablemicrocarriers are made of synthetic polymers, non-limiting examples ofwhich include, among others, polylactide (PLA), polyglycolide (PGA),poly(lactide-co-glycolide) (PLGA), poly(caprolactone), polydioxanonetrimethylene carbonate, polyhybroxyalkonates (e.g.,poly(hydroxybutyrate), poly(ethyl glutamate), poly(DTHiminocarbony(bisphenol A iminocarbonate), poly(ortho ester), andpolycyanoacrylates.

In some aspects, the microcarriers comprise hydrogels, which aretypically hydrophilic polymer networks filled with water. Hydrogels havethe advantage of selective trigger of polymer swelling. Depending on thecomposition of the polymer network, swelling of the microparticle may betriggered by a variety of stimuli, including pH, ionic strength,thermal, electrical, ultrasound, and enzyme activities. Non-limitingexamples of polymers useful in hydrogel compositions include, amongothers, those formed from polymers of poly(lactide-co-glycolide);poly(N-isopropylacrylamide); poly(methacrylic acid-g-polyethyleneglycol); polyacrylic acid and poly(oxypropylene-co-oxyethylene) glycol;and natural compounds such as chrondroitan sulfate, chitosan, gelatin,fibrinogen, or mixtures of synthetic and natural polymers, for examplechitosan-poly (ethylene oxide). The polymers may be crosslinkedreversibly or irreversibly to form gels adaptable for forming threedimensional tissues.

In exemplary aspects, the microcarriers or beads for use in the presentinvention are composed wholly or composed partly of dextran.

In accordance with the present invention the culturing method isapplicable to proliferation of different types of cells, includingstromal cells, such as fibroblasts, and particularly primary humanneonatal foreskin fibroblasts. In various aspects, the cells inoculatedonto the scaffold or framework can be stromal cells comprisingfibroblasts, with or without other cells, as further described below. Insome embodiments, the cells are stromal cells that are typically derivedfrom connective tissue, including, but not limited to: (1) bone; (2)loose connective tissue, including collagen and elastin; (3) the fibrousconnective tissue that forms ligaments and tendons, (4) cartilage; (5)the ECM of blood; (6) adipose tissue, which comprises adipocytes; and(7) fibroblasts.

Stromal cells can be derived from various tissues or organs, such asskin, heart, blood vessels, bone marrow, skeletal muscle, liver,pancreas, brain, foreskin, which can be obtained by biopsy (whereappropriate) or upon autopsy. In one aspect, fetal fibroblasts can beobtained in high quantity from foreskin, such as neonatal foreskins.

In some aspects, the cells comprise fibroblasts, which can be from afetal, neonatal, adult origin, or a combination thereof. In someaspects, the stromal cells comprise fetal fibroblasts, which can supportthe growth of a variety of different cells and/or tissues. As usedherein, a fetal fibroblast refers to fibroblasts derived from fetalsources. As used herein, neonatal fibroblast refers to fibroblastsderived from newborn sources. Under appropriate conditions, fibroblastscan give rise to other cells, such as bone cells, fat cells, and smoothmuscle cells and other cells of mesodermal origin. In some embodiments,the fibroblasts comprise dermal fibroblasts, which are fibroblastsderived from skin. Normal human dermal fibroblasts can be isolated fromneonatal foreskin. These cells are typically cryopreserved at the end ofthe primary culture.

In other aspects, the three-dimensional tissue can be made using stem orprogenitor cells, either alone, or in combination with any of the celltypes discussed herein. Stem and progenitor cells include, by way ofexample and not limitation, embryonic stem cells, hematopoietic stemcells, neuronal stem cells, epidermal stem cells, and mesenchymal stemcells.

In some embodiments, a “specific” three-dimensional tissue can beprepared by inoculating the three-dimensional scaffold with cellsderived from a particular organ, i.e., skin, heart, and/or from aparticular individual who is later to receive the cells and/or tissuesgrown in culture in accordance with the methods described herein.

For certain uses in vivo it is preferable to obtain the stromal cellsfrom the patient's own tissues. The growth of cells in the presence ofthe three-dimensional stromal support framework can be further enhancedby adding to the framework, or coating the framework support withproteins, e.g., collagens, laminins, elastic fibers, reticular fibers,glycoproteins; glycosaminoglycans, e.g., heparin sulfate,chondroitin-4-sulfate, chondroitin-6-sulfate, dermatan sulfate, keratansulfate, etc.; a cellular matrix, and/or other materials.

Thus, since the two-dimensional or three-dimensional culture systemsdescribed herein are suitable for growth of diverse cell types andtissues, and depending upon the tissue to be cultured and the collagentypes desired, the appropriate stromal cells may be selected toinoculate the framework.

While the methods and applications of the present invention are suitablefor use with different cell types, such as tissue specific cells ordifferent types of stromal cells as discussed herein, derivation of thecells for use with the present invention may also be species specific.Accordingly, ECM compositions may be generated that are speciesspecific. For example, the cells for use in the present invention mayinclude human cells. For example, the cells may be human fibroblasts.Likewise, the cells are from another species of animal, such as equine(horse), canine (dog) or feline (cat) cells. Additionally, cells fromone species or strain of species may be used to generate ECMcompositions for use in other species or related strains (e.g.,allogeneic, syngeneic and xenogeneic). It is also to be appreciated thatcells derived from various species may be combined to generatemulti-species ECM compositions.

Accordingly, the methods and compositions of the present invention aresuitable in applications involving non-human animals. As used herein,“veterinary” refers to the medical science concerned or connected withthe medical or surgical treatment of animals, especially domesticanimals. Common veterinary animals may include mammals, amphibians,avians, reptiles and fishes. For example, typical mammals may includedogs, cats, horses, rabbits, primates, rodents, and farm animals, suchas cows, horses, goats, sheep, and pigs.

As discussed above, additional cells may be present in the culture withthe stromal cells. These additional cells may have a number ofbeneficial effects, including, among others, supporting long term growthin culture, enhancing synthesis of growth factors, and promotingattachment of cells to the scaffold. Additional cell types include asnon-limiting examples, smooth muscle cells, cardiac muscle cells,endothelial cells, skeletal muscle cells, endothelial cells, pericytes,macrophages, monocytes, and adipocytes. Such cells may be inoculatedonto the framework along with fibroblasts, or in some aspects, in theabsence of fibroblasts. These stromal cells may be derived fromappropriate tissues or organs, including, by way of example and notlimitation, skin, heart, blood vessels, bone marrow, skeletal muscle,liver, pancreas, and brain. In other aspects, one or more other celltypes, excluding fibroblasts, are inoculated onto the scaffold. In stillother aspects, the scaffolds are inoculated only with fibroblast cells.

Fibroblasts may be readily isolated by disaggregating an appropriateorgan or tissue which is to serve as the source of the fibroblasts. Forexample, the tissue or organ can be disaggregated mechanically and/ortreated with digestive enzymes and/or chelating agents that weaken theconnections between neighboring cells making it possible to disperse thetissue into a suspension of individual cells without appreciable cellbreakage. Enzymatic dissociation can be accomplished by mincing thetissue and treating the minced tissue with any of a number of digestiveenzymes either alone or in combination. These include but are notlimited to trypsin, chymotrypsin, collagenase, elastase, hyaluronidase,DNase, pronase, and/or dispase etc. Mechanical disruption can also beaccomplished by a number of methods including, but not limited to theuse of grinders, blenders, sieves, homogenizers, pressure cells, orinsonators to name but a few. In one aspect, excised foreskin tissue istreated using digestive enzymes, typically collagenase and/or trypsinaseto disassociate the cells from encapsulating structures.

The isolation of fibroblasts, for example, can be carried out asfollows: fresh tissue samples are thoroughly washed and minced in Hanks'balanced salt solution (HBSS) in order to remove serum. The mincedtissue is incubated from 1-12 hours in a freshly prepared solution of adissociating enzyme such as trypsin. After such incubation, thedissociated cells are suspended, pelleted by centrifugation and platedonto culture dishes. All fibroblasts will attach before other cells,therefore, appropriate stromal cells can be selectively isolated andgrown. The isolated fibroblasts can then be grown to confluency, liftedfrom the confluent culture and inoculated onto the three-dimensionalframework, see Naughton et al., 1987, J. Med. 18(3&4):219-250.Inoculation of the three-dimensional framework with a high concentrationof stromal cells, e.g., approximately 10⁶ to 5×10⁷ cells/ml, will resultin the establishment of the three-dimensional stromal support in shorterperiods of time.

Once the tissue has been reduced to a suspension of individual cells,the suspension can be fractionated into subpopulations from which thefibroblasts and/or other stromal cells and/or elements can be obtained.This also may be accomplished using standard techniques for cellseparation including, but not limited to, cloning and selection ofspecific cell types, selective destruction of unwanted cells (negativeselection), separation based upon differential cell agglutinability inthe mixed population, freeze-thaw procedures, differential adherenceproperties of the cells in the mixed population, filtration,conventional and zonal centrifugation, centrifugal elutriation(counter-streaming centrifugation), unit gravity separation,countercurrent distribution, electrophoresis and fluorescence-activatedcell sorting. For a review of clonal selection and cell separationtechniques, see Freshney, Culture of Animal Cells. A Manual of BasicTechniques, 2d Ed., A. R. Liss, Inc., New York, 1987, Ch. 11 and 12, pp.137-168.

In one aspect, isolated fibroblast cells can be grown to produce cellbanks. Cell banks are created to allow for initiating various quantitiesand timing of cultivation batches and to allow preemptive testing ofcells for contaminants and specific cellular characteristics.Fibroblasts from the cell banks are subsequently grown to increase cellnumber to appropriate levels for seeding scaffolds. Operations involvingenvironmental exposure of cells and cell contacting materials areperformed by aseptic practices to reduce the potential for contaminationof foreign materials or undesirable microbes.

In another aspect of the invention, after isolation, cells can be grownthrough several passages to a quantity suitable for building master cellbanks. The cell banks can then be, harvested and filled into appropriatevessels and preserved in cryogenic conditions. Cells in frozen vialsfrom master cell banks can be thawed and grown through additionalpassages (usually two or more). The cells can then be used to preparecryogenically preserved working cell banks.

A cell expansion step uses vials of cells at the working cell bank stageto further increase cell numbers for inoculating three-dimensionalscaffolds or supports, such as mesh or microcarriers. Each passage is aseries of sub-culture steps that include inoculating cell growthsurfaces, incubation, feeding the cells and harvesting.

Cultivation for cell banks and cell expansion can be conducted byinoculating culture vessels, such as culture flasks, roller bottles ormicrocarriers. Stromal cells, such as fibroblasts, attach to theintended growth surfaces and grow in the presence of culture media.Culture vessels, such as culture flasks, roller bottles andmicrocarriers are specifically configured for cell culture and arecommonly made from various plastic materials qualified for intendedapplications. Microcarriers typically are microscopic or macroscopicbeads and are typically made of various plastic materials. However, theycan be made from other materials such as glasses or solid/semi-solidbiologically based materials such as collagens or other materials suchas Dextran, a modified sugar complex as discussed above.

During cultivation, expended media is periodically replaced with freshmedia during the course of cell growth to maintain adequate availabilityof nutrients and removal of inhibitory products of cultivation. Cultureflasks and roller bottles provide a surface for the cells to grow ontoand are typically used for cultivation of anchorage dependent cells.

In one aspect, incubation is performed in a chamber heated at 37° C.Cultivation topologies requiring communication of media and the chamberenvironment use a 5% CO₂ v/v with air in the chamber gas space to aid inregulation of pH. Alternately, vessels equipped to maintain cultivationtemperature and pH can be used for both cell expansion and ECMproduction operations. Temperatures below 35° C. or above 38° C. and CO₂concentrations below 3% or above 12% may not be appropriate.

Harvesting cells from attachment surfaces can conducted by removal ofgrowth media and rinsing the cells with a buffered salt solution toreduce enzyme competing protein, application of disassociating enzymesthen neutralization of the enzymes after cell detachment. Harvested cellsuspension is collected and harvest fluids are separated bycentrifugation. Cell suspensions from sub-culture harvests can besampled to assess the quantity of cells recovered and other cellularattributes and are subsequently combined with fresh media and applied asinoculums. The number of passages used for preparing cell banks andscaffold inoculum is critical with regard to achieving acceptable ECMcharacteristics.

After an appropriate three-dimensional scaffold is prepared, it isinoculated by seeding with the prepared stromal cells. Inoculation ofthe scaffold may be done in a variety of ways, such as sedimentation.Mesh prepared for culture of ECM under aerobic conditions are preparedin the same manner as for hypoxic grown mesh with the exception that ananaerobic chamber is not used to create hypoxic conditions.

For example, for both mesh prepared for culture of ECM under bothaerobic and hypoxic conditions, prepared and sterilized mesh is placedin sterile 150 mm diameter×15 mm deep petri dishes and stacked to athickness of approximately 10 pieces. Stacks of mesh are then inoculatedby sedimentation. Cells are added to fresh media to obtain theappropriate concentration of cells for inoculum. Inoculum is added tothe stack of mesh where cells settle onto the nylon fibers and attachwhile in incubated conditions. After an adequate time, individuallyseeded mesh sheets can be aseptically separated from the stack andplaced individually into separate 150 mm×15 mm petri dishes containingapproximately 50 ml of growth media.

Incubation of the inoculated culture is performed under hypoxicconditions, which is discovered to produce an ECM and surrounding mediawith unique properties as compared to ECM generated under normal cultureconditions. As used herein, hypoxic conditions are characterized by alower oxygen concentration as compared to the oxygen concentration ofambient air (approximately 15%-20% oxygen). In one aspect, hypoxicconditions are characterized by an oxygen concentration less than about10%. In another aspect hypoxic conditions are characterized by an oxygenconcentration of about 1% to 10%, 1% to 9%, 1% to 8%, 1% to 7%, 1% to6%, 1% to 5%, 1% to 4%, 1% to 3%, or 1% to 2%. In a certain aspect, thesystem maintains about 1-3% oxygen within the culture vessel. Hypoxicconditions can be created and maintained by using a culture apparatusthat allows one to control ambient gas concentrations, for example, ananaerobic chamber.

Incubation of cell cultures is typically performed in normal atmospherewith 15-20% oxygen and 5% CO₂ for expansion and seeding, at which pointlow oxygen cultures are split to an airtight chamber that is floodedwith 95% nitrogen/5% CO₂ so that a hypoxic environment is created withinthe culture medium.

For example, petri dishes with mesh cultured for producing ECM underhypoxic conditions are initially grown in incubation at 37° C. and 95%air/5% CO₂ for 2-3 weeks. Following the period of near atmosphericcultivation, the petri dishes of mesh are incubated in a chamberdesigned for anaerobic cultivation that is purged with a gas mixture ofapproximately 95% nitrogen and 5% CO₂. Expended growth media is replacedwith fresh media at atmospheric oxygen level through the culture periodand after media is exchanged the mesh filled petri dishes are place inthe anaerobic chamber, the chamber is purged with 95% nitrogen/5% CO₂then incubated at 37° C. Cultured mesh are harvested when they reach thedesired size or contain the desire biological components.

During the incubation period, the stromal cells will grow linearly alongand envelop the three-dimensional framework before beginning to growinto the openings of the framework. The growing cells produce a myriadof growth factors, regulatory factors and proteins, some of which aresecreted in the surrounding media, and others that are deposited on thesupport to make up the ECM more fully discussed below. Growth andregulatory factors can be added to the culture, but are not necessary.Culture of the stromal cells produces both non-soluble and solublefractions. The cells are grown to an appropriate degree to allow foradequate deposition of ECM proteins.

During culturing of the three-dimensional tissues, proliferating cellsmay be released from the framework and stick to the walls of the culturevessel where they may continue to proliferate and form a confluentmonolayer. To minimize this occurrence, which may affect the growth ofcells, released cells may be removed during feeding or by transferringthe three-dimensional cell culture to a new culture vessel. Removal ofthe confluent monolayer or transfer of the cultured tissue to freshmedia in a new vessel maintains or restores proliferative activity ofthe three-dimensional cultures. In some aspects, removal or transfersmay be done in a culture vessel which has a monolayer of cultured cellsexceeding 25% confluency. Alternatively, the culture in some embodimentsis agitated to prevent the released cells from sticking; in others,fresh media is infused continuously through the system. In some aspects,two or more cell types can be cultured together either at the same timeor one first followed by the second (e.g., fibroblasts and smooth musclecells or endothelial cells).

After inoculation of the three dimensional scaffolds, the cell cultureis incubated in an appropriate nutrient medium and incubation conditionsthat supports growth of cells into the three dimensional tissues. Manycommercially available media such as Dulbecco's Modified Eagles Medium(DMEM), RPMI 1640, Fisher's, Iscove's, and McCoy's, may be suitable forsupporting the growth of the cell cultures. The medium may besupplemented with additional salts, carbon sources, amino acids, serumand serum components, vitamins, minerals, reducing agents, bufferingagents, lipids, nucleosides, antibiotics, attachment factors, and growthfactors. Formulations for different types of culture media are describedin various reference works available to the skilled artisan (e.g.,Methods for Preparation of Media, Supplements and Substrates for SerumFree Animal Cell Cultures, Alan R. Liss, New York (1984); TissueCulture: Laboratory Procedures, John Wiley & Sons, Chichester, England(1996); Culture of Animal Cells, A Manual of Basic Techniques, 4 th Ed.,Wiley-Liss (2000)).

The growth or culture media used in any of the culturing steps of thepresent invention, whether under aerobic or hypoxic conditions, mayinclude serum, or be serum free. In one aspect, the media is Dulbecco'sModified Eagle Medium with 4.5 g/L glucose, alanyl-L-glutamine, Eq 2 mM,and nominally supplemented with 10% fetal bovine serum. In anotheraspect, the media is a serum free media and is Dulbecco's Modified EagleMedium with 4.5 g/L glucose base medium with Glutamax®, supplementedwith 0.5% serum albumin, 2 μg/ml heparin, 1 μg/ml recombinant basic FGF,1 μg/ml soybean trypsin inhibitor, 1X ITS supplement(insulin-transferrin-selenium, Sigma Cat. No. 13146), 1:1000 dilutedfatty acid supplement (Sigma Cat. No. 7050), and 1:1000 dilutedcholesterol. Additionally, the same media can be used for both hypoxicand aerobic cultivation. In one aspect, the growth media is changed fromserum based media to serum free media after seeding and the first weekof growth.

Incubation conditions will be under appropriate conditions of pH,temperature, and gas (e.g., O₂, CO₂, etc) to maintain an hypoxic growthcondition. In some embodiments, the three-dimensional cell culture canbe suspended in the medium during the incubation period in order tomaximize proliferative activity and generate factors that facilitate thedesired biological activities of the fractions. In addition, the culturemay be “fed” periodically to remove the spent media, depopulate releasedcells, and add new nutrient source. During the incubation period, thecultured cells grow linearly along and envelop the filaments of thethree-dimensional scaffold before beginning to grow into the openings ofthe scaffold.

During incubation under hypoxic conditions, as compared to incubationunder normal atmospheric oxygen concentrations of about 15-20%,thousands of genes are differentially expressed. Several genes have beenfound to be upregulated or downregulated in such compositions, mostnotably certain laminin species, collagen species and Wnt factors. Invarious aspects, the three dimensional ECM may be defined by thecharacteristic fingerprint or suite of cellular products produced by thecells due to growth in hypoxic condition as compared with growth undernormal conditions. In the ECM compositions specifically exemplifiedherein, the three-dimensional tissues and surrounding media arecharacterized by expression and/or secretion of various factors.

The three dimensional tissues and compositions described herein have ECMthat is present on the scaffold or framework. In some aspects, the ECMincludes various laminin and collagen types due to growth under hypoxicconditions and selection of cells grown on the support. The proportionsof ECM proteins deposited can be manipulated or enhanced by selectingfibroblasts which elaborate the appropriate collagen type as well asgrowing the cells under hypoxic conditions in which expression ofspecific laminin and collagen species are upregulated or down-regulated.

Selection of fibroblasts can be accomplished in some aspects usingmonoclonal antibodies of an appropriate isotype or subclass that defineparticular collagen types. In other aspects, solid substrates, such asmagnetic beads, may be used to select or eliminate cells that have boundantibody. Combination of these antibodies can be used to select(positively or negatively) the fibroblasts which express the desiredcollagen type. Alternatively, the stroma used to inoculate the frameworkcan be a mixture of cells which synthesize the desired collagen types.The distribution and origins of the exemplary type of collagen are shownin Table I.

TABLE 1 Distributions and Origins of Various Types of Collagen CollagenType Principle Tissue Distribution Cells of Origin I Loose and denseordinary Fibroblasts and reticular connective tissue; collagen cells;smooth muscle cells fibers Fibrocartilage Bone Osteoblasts DentinOdontoblasts II Hyaline and elastic cartilage Chondrocytes Vitreous bodyof eye Retinal cells III Loose connective tissue; Fibroblasts andreticular reticular fibers cells Papillary layer of dermis Smooth musclecells; endothelial cells Blood vessels IV Basement membranes Epithelialand endothelial cells Lens capsule of eye Lens fibers V Fetal membranes;placenta Fibroblasts Basement membranes Bone Smooth muscle Smooth musclecells IV Basement membranes Epithelial and endothelial cells Lenscapsule of the eye Lens fiber V Fetal membranes; placenta FibroblastsBasement membranes Bone Smooth muscle Smooth muscle cells VI Connectivetissue Fibroblasts VII Epithelial basement Fibroblasts membranesanchoring fibrils keratinocytes VIII Cornea Corneal fibroblasts IXCartilage X Hypertrophic cartilage XI Cartilage XII Papillary dermisFibroblasts XIV Reticular dermis Fibroblasts (undulin) XVII P170 bullouspemphigoid Keratinocytes antigen

Additional types of collagen that may be present in ECM compositions areshown in Table 2.

TABLE 2 Types of Collagen and Corresponding Gene(s) Collagen TypeGene(s) I COL1A1, COL1A2 II COL2A1 III COL3A1 IV COL4A1, COL4A2, COL4A3,COL4A4, COL4A5, COL4A6 V COL5A1, COL5A2, COL5A3 VI COL6A1, COL6A2,COL6A3 VII COL7A1 VIII COL8A1, COL8A2 IX COL9A1, COL9A2, COL9A3 XCOL10A1 XI COL11A1, COL11A2 XII COL12A1 XIII COL13A1 XIV COL14A1 XVCOL15A1 XVI COL16A1 XVII COL17A1 XVIII COL18A1 XIX COL19A1 XX COL20A1XXI COL21A1 XXII COL22A1 XXIII COL23A1 XXIV COL24A1 XXV COL25A1 XXVIEMID2 XXVII COL27A1 XXVIII COL28A1

As discussed above the ECM compositions described herein include variouscollagens. As shown in Table 3 of Example 1, expression of severalspecies of collagen are found to be upregulated in hypoxic cultured ECMcompositions. Accordingly, in one aspect of the present invention, theECM composition including one or more embryonic proteins, includesupregulation of collagen species as compared with that produced inoxygen conditions of about 15-20% oxygen. In another aspect, theupregulated collagen species are type V alpha 1; IX alpha 1; IX alpha 2;VI alpha 2; VIII alpha 1; IV, alpha 5; VII alpha 1; XVIII alpha 1; andXII alpha 1.

In addition to various collagens, the ECM composition described hereininclude various laminins. Laminins are a family of glycoproteinheterotrimers composed of an alpha, beta, and gamma chain subunit joinedtogether through a coiled-coil domain. To date, 5 alpha, 4 beta, and 3gamma laminin chains have been identified that can combine to form 15different isoforms. Within this structure are identifiable domains thatpossess binding activity towards other laminin and basal laminamolecules, and membrane-bound receptors. Domains VI, IVb, and IVa formglobular structures, and domains V, IIIb, and IIIc (which containcysteine-rich EGF-like elements) form rod-like structures. Domains I andII of the three chains participate in the formation of a triple-strandedcoiled-coil structure (the long arm).

Laminin chains possess shared and unique functions and are expressedwith specific temporal (developmental) and spatial (tissue-sitespecific) patterns. The laminin alpha-chains are considered to be thefunctionally important portion of the heterotrimers, as they exhibittissue-specific distribution patterns and contain the major cellinteraction sites. Vascular endothelium is known to express two lamininisoforms, with varied expression depending on the developmental stage,vessel type, and the activation state of the endothelium.

Accordingly, in one aspect of the present invention, the ECM compositionincluding one or more embryonic proteins, includes upregulation ordownregulation of various laminin species as compared with that producedin oxygen conditions of about 15-20% oxygen.

Laminin 8, is composed of alpha-4, beta-1, and gamma-1 laminin chains.The laminin alpha-4 chain is widely distributed both in adults andduring development. In adults it can be identified in the basementmembrane surrounding cardiac, skeletal, and smooth muscle fibers, and inlung alveolar septa. It is also known to exist in the endothelialbasement membrane both in capillaries and larger vessels, and in theperineurial basement membrane of peripheral nerves, as well as inintersinusoidal spaces, large arteries, and smaller arterioles of bonemarrow. Laminin 8 is a major laminin isoform in the vascular endotheliumthat is expressed and adhered to by platelets and is synthesized in3T3-L1 adipocytes, with its level of synthesis shown to increase uponadipose conversion of the cells. Laminin 8 is thought to be the lamininisoform generally expressed in mesenchymal cell lineages to inducemicrovessels in connective tissues. Laminin 8 has also been identifiedin mouse bone marrow primary cell cultures, arteriolar walls, andintersinusoidal spaces where it is the major laminin isoform in thedeveloping bone marrow. Due to its localization in adult bone marrowadjacent to hematopoietic cells, laminin isoforms containing the alpha-4chain are likely to have biologically relevant interactions withdeveloping hematopoietic cells.

Accordingly, in another aspect of the present invention the ECM includesupregulation of laminin species, such as laminin 8. In another aspect,laminins produced by the three dimensional tissues of the presentinvention, includes at least laminin 8, which defines a characteristicor signature of the laminin proteins present in the composition.

The ECM compositions described herein can include various Wnt factors.Wnt family factors are signaling molecules having roles in a myriad ofcellular pathways and cell-cell interaction processes. Wnt signaling hasbeen implicated in tumorigenesis, early mesodermal patterning of theembryo, morphogenesis of the brain and kidneys, regulation of mammarygland proliferation, and Alzheimer's disease. As shown in Table 4 ofExample 1, expression of several species of Wnt proteins are found to beupregulated in hypoxic cultured ECM compositions. Accordingly, in oneaspect of the present invention, the ECM composition including one ormore embryonic proteins, includes upregulation of Wnt species ascompared with that produced in oxygen conditions of about 15-20% oxygen.In another aspect, the upregulated Wnt species are wnt 7a and wnt 11. Inanother aspect, Wnt factors produced by the three dimensional tissues ofthe present invention, include at least wnt7a, and wnt11, which definesa characteristic or signature of the Wnt proteins present in thecomposition.

The culturing methods described herein, including culture under hypoxicconditions, have also been shown to upregulate expression of variousgrowth factors. Accordingly, the ECM compositions described herein caninclude various growth factors, such as a vascular endothelial growthfactor (VEGF). As used herein, a VEGF in intended to include all knownVEGF family members. VEGFs are a sub-family of growth factors, morespecifically of platelet-derived growth factor family of cystine-knotgrowth factors. VEGFs have a well known role in both vasculogenesis andangiogenesis. Several VEGFs are known, including VEGF-A, which wasformerly known as VEGF before the discovery of other VEGF species. OtherVEGF species include placenta growth factor (PlGF), VEGF-B, VEGF-C andVEGF-D. Additionally, several isoforms of human VEGF are well known.

In accordance with the increased production of Wnt proteins as well asgrowth factors by culturing under hypoxic conditions as describedherein, the present invention further provides a method of producing aWnt protein and a vascular endothelial growth factor (VEGF). The methodcan include culturing cells under hypoxic conditions as describedherein, on a three-dimensional surface in a suitable growth medium, toproduce the Wnt protein and the VEGF. In an exemplary aspect, the Wntspecies are wnt 7a and wnt 11 and the VEGF is VEGF-A. The proteins maybe further processed or harvested as described further herein or bymethods known in the art.

A discussed throughout, the ECM compositions of the present inventionincludes both soluble and non-soluble fractions or any portion thereof.It is to be understood that the compositions of the present inventionmay include either or both fractions, as well as any combinationthereof. Additionally, individual components may be isolated from thefractions to be used individually or in combination with other isolatesor known compositions.

Accordingly, in various aspects, ECM compositions produced using themethods of the present invention may be used directly or processed invarious ways, the methods of which may be applicable to both thenon-soluble and soluble fractions. The soluble fraction, including thecell-free supernatant and media, may be subject to lyophilization forpreserving and/or concentrating the factors. Various biocompatiblepreservatives, cryoprotectives, and stabilizer agents may be used topreserve activity where required. Examples of biocompatible agentsinclude, among others, glycerol, dimethyl sulfoxide, and trehalose. Thelyophilizate may also have one or more excipients such as buffers,bulking agents, and tonicity modifiers. The freeze-dried media may bereconstituted by addition of a suitable solution or pharmaceuticaldiluent, as further described below.

In other aspects, the soluble fraction is dialyzed. Dialysis is one ofthe most commonly used techniques to separate sample components based onselective diffusion across a porous membrane. The pore size determinesmolecular-weight cutoff (MWCO) of the membrane that is characterized bythe molecular-weight at which 90% of the solute is retained by themembrane. In certain aspects membranes with any pore size iscontemplated depending on the desired cutoff. Typical cutoffs are 5,000Daltons, 10,000 Daltons, 30,000 Daltons, and 100,000 Daltons, howeverall sizes are contemplated.

In some aspects, the soluble fraction may be processed by precipitatingthe active components (e.g., growth factors) in the media. Precipitationmay use various procedures, such as salting out with ammonium sulfate oruse of hydrophilic polymers, for example polyethylene glycol.

In other aspects, the soluble fraction is subject to filtration usingvarious selective filters. Processing the soluble fraction by filteringis useful in concentrating the factors present in the fraction and alsoremoving small molecules and solutes used in the soluble fraction.Filters with selectivity for specified molecular weights include <5000Daltons, <10,000 Daltons, and <15,000 Daltons. Other filters may be usedand the processed media assayed for therapeutic activity as describedherein. Exemplary filters and concentrator system include those basedon, among others, hollow fiber filters, filter disks, and filter probes(see, e.g., Amicon Stirred Ultrafiltration Cells).

In still other aspects, the soluble fraction is subject tochromatography to remove salts, impurities, or fractionate variouscomponents of the medium. Various chromatographic techniques may beemployed, such as molecular sieving, ion exchange, reverse phase, andaffinity chromatographic techniques. For processing conditioned mediumwithout significant loss of bioactivity, mild chromatographic media maybe used. Non-limiting examples include, among others, dextran, agarose,polyacrylamide based separation media (e.g., available under varioustradenames, such as Sephadex, Sepharose, and Sephacryl).

In still other aspects, the conditioned media is formulated asliposomes. The growth factors may be introduced or encapsulated into thelumen of liposomes for delivery and for extending life time of theactive factors. As known in the art, liposomes can be categorized intovarious types: multilamellar (MLV), stable plurilamellar (SPLV), smallunilamellar (SUV) or large unilamellar (LUV) vesicles. Liposomes can beprepared from various lipid compounds, which may be synthetic ornaturally occurring, including phosphatidyl ethers and esters, such asphosphotidylserine, phosphotidylcholine, phosphatidyl ethanolamine,phosphatidylinositol, dimyristoylphosphatidylcholine; steroids such ascholesterol; cerebrosides; sphingomyelin; glycerolipids; and otherlipids (see, e.g., U.S. Pat. No. 5,833,948).

The soluble fraction may be used directly without additional additives,or prepared as pharmaceutical compositions with various pharmaceuticallyacceptable excipients, vehicles or carriers. A “pharmaceuticalcomposition” refers to a form of the soluble and/or non-solublefractions and at least one pharmaceutically acceptable vehicle, carrier,or excipient. For intradermal, subcutaneous or intramuscularadministration, the compositions may be prepared in sterile suspension,solutions or emulsions of the ECM compositions in aqueous or oilyvehicles. The compositions may also contain formulating agents, such assuspending, stabilizing or dispersing agents. Formulations for injectionmay be presented in unit dosage form, ampules in multidose containers,with or without preservatives. Alternatively, the compositions may bepresented in powder form for reconstitution with a suitable vehicleincluding, by way of example and not limitation, sterile pyrogen freewater, saline, buffer, or dextrose solution.

In other aspects, the three dimensional tissues are cryopreservedpreparations, which are thawed prior to use. Pharmaceutically acceptablecryopreservatives include, among others, glycerol, saccharides, polyols,methylcellulose, and dimethyl sulfoxide. Saccharide agents includemonosaccharides, disaccharides, and other oligosaccharides with glasstransition temperature of the maximally freeze-concentrated solution(Tg) that is at least -60, -50, -40, -30, -20, -10, or 0° C. Anexemplary saccharide for use in cryopreservation is trehalose.

In some aspects, the three dimensional tissues are treated to kill thecells prior to use. In some aspects, the ECM deposited on the scaffoldsmay be collected and processed for administration (see U.S. Pat. Nos.5,830,708 and 6,280,284, incorporated herein by reference).

In other embodiments, the three dimensional tissue may be concentratedand washed with a pharmaceutically acceptable medium for administration.Various techniques for concentrating the compositions are available inthe art, such as centrifugation or filtering. Examples include, dextransedimentation and differential centrifugation. Formulation of the threedimensional tissues may also involve adjusting the ionic strength of thesuspension to isotonicity (i.e., about 0.1 to 0.2) and to physiologicalpH (i.e., pH 6.8 to 7.5). The formulation may also contain lubricants orother excipients to aid in administration or stability of the cellsuspension. These include, among others, saccharides (e.g., maltose) andorganic polymers, such as polyethylene glycol and hyaluronic acid.Additional details for preparation of various formulations are describedin U.S. Patent Publication No. 2002/0038152, incorporated herein byreference.

As discussed above, the ECM compositions of the present invention may beprocessed in a number of ways depending on the anticipated applicationand appropriate delivery or administration of the ECM composition. Forexample, the compositions may be delivered as three-dimensionalscaffolds or implants, or the compositions may be formulated forinjection as described above. The terms “administration” or“administering” are defined to include an act of providing a compound orpharmaceutical composition of the invention to a subject in need oftreatment. The phrases “parenteral administration” and “administeredparenterally” as used herein means modes of administration other thanenteral and topical administration, usually by injection, and includes,without limitation, intravenous, intramuscular, intraarterial,intrathecal, intracapsular, intraorbital, intracardiac, intradermal,intraperitoneal, transtracheal, subcutaneous, subcuticular,intraarticulare, subcapsular, subarachnoid, intraspinal and intrasternalinjection and infusion. The phrases “systemic administration,”“administered systemically,” “peripheral administration” and“administered peripherally” as used herein mean the administration of acompound, drug or other material other than directly into the centralnervous system, such that it enters the subject's system and, thus, issubject to metabolism and other like processes, for example,subcutaneous administration.

The term “subject” as used herein refers to any individual or patient towhich the subject methods are performed. Generally the subject is human,although as will be appreciated by those in the art, the subject may bean animal. Thus other animals, including mammals such as rodents(including mice, rats, hamsters and guinea pigs), cats, dogs, rabbits,farm animals including cows, horses, goats, sheep, pigs, etc., andprimates (including monkeys, chimpanzees, orangutans and gorillas) areincluded within the definition of subject.

The ECM compositions of the present invention have a variety ofapplications including, but not limited to, promoting repair and/orregeneration of damaged cells or tissues, use in patches to promotetissue regeneration, use in tissue culture systems for culturing cells,such as stem cells, use in surface coatings used in association withimplantable devices (e.g., pacemakers, stents, stent grafts, vascularprostheses, heart valves, shunts, drug delivery ports or catheters),promoting soft tissue repair, augmentation, and/or improvement of a skinsurface, such as wrinkles, use as a biological anti-adhesion agent or asa biological vehicle for cell delivery or maintenance at a site ofdelivery.

Additionally, the ECM compositions derived from culturing cells asdescribed in any method herein, may be used in any other application ormethod of the present invention. For example, the ECM compositionsgenerated by culturing cells using the tissue culture system of thepresent invention may be used, for example, in the repair and/orregeneration of cells, use in patches to promote tissue regeneration,use in tissue culture systems for culturing cells, such as stem cells,use in surface coatings used in association with implantable devices(e.g., pacemakers, stents, stent grafts, vascular prostheses, heartvalves, shunts, drug delivery ports or catheters), promoting soft tissuerepair, augmentation, and/or improvement of a skin surface, such aswrinkles, use as a biological anti-adhesion agent or as a biologicalvehicle for cell delivery or maintenance at a site of delivery.

In various embodiments, the present invention includes methods forrepair and/or regeneration of cells or tissue and promoting soft tissuerepair. One embodiment includes a method of repair and/or regenerationof cells by contacting cells to be repaired or regenerated with the ECMcompositions of the present invention. The method may be used for repairand/or regeneration of a variety of cells as discussed herein, includingosteochondral cells.

In one aspect, the method contemplates repair of osteochondral defects.As used herein, “osteochondral cells” refers to cells which belong toeither the chondrogenic or osteogenic lineage or which can undergodifferentiation into either the chondrogenic or osteogenic lineage,depending on the environmental signals. This potential can be tested invitro or in vivo by known techniques. Thus, in one aspect, the ECMcompositions of the present invention are used to repair and/orregenerate, chondrogenic cells, for example, cells which are capable ofproducing cartilage or cells which themselves differentiate into cellsproducing cartilage, including chondrocytes and cells which themselvesdifferentiate into chondrocytes (e.g., chondrocyte precursor cells).Thus, in another aspect, the compositions of the present invention areuseful in repair and/or regeneration of connective tissue. As usedherein, “connective tissue” refers to any of a number of structuraltissues in the body of a mammal including but not limited to bone,cartilage, ligament, tendon, meniscus, dermis, hyperdermis, muscle,fatty tissue, joint capsule.

The ECM compositions of the present invention may be used for treatingosteochondral defects of a diarthroidal joint, such as knee, an ankle,an elbow, a hip, a wrist, a knuckle of either a finger or toe, or atemperomandibular joint. Such osteochondral defects can be the result oftraumatic injury (e.g., a sports injury or excessive wear) or a diseasesuch as osteoarthritis. A particular aspect relates to the use of thematrix of the present invention in the treatment or prevention ofsuperficial lesions of osteoarthritic cartilage. Additionally thepresent invention is of use in the treatment or prevention ofosteochondral defects which result from ageing or from giving birth.Osteochondral defects in the context of the present invention shouldalso be understood to comprise those conditions where repair ofcartilage and/or bone is required in the context of surgery such as, butnot limited to, cosmetic surgery (e.g., nose, ear). Thus such defectscan occur anywhere in the body where cartilage or bone formation isdisrupted or where cartilage or bone are damaged or non-existent due toa genetic defect.

As discussed above, growth factors or other biological agents whichinduce or stimulate growth of particular cells may be included in theECM compositions of the present invention. The type of growth factorswill be dependent on the cell-type and application for which thecomposition is intended. For example, in the case of osteochondralcells, additional bioactive agents may be present such as cellulargrowth factors (e.g., TGF-β), substances that stimulate chondrogenesis(e.g., BMPs that stimulate cartilage formation such as BMP-2, BMP-12 andBMP-13), factors that stimulate migration of stromal cells to thescaffold, factors that stimulate matrix deposition, anti-inflammatories(e.g., non-steroidal anti-inflammatories), immunosuppressants (e.g.,cyclosporin). Other proteins may also be included, such as other growthfactors such as platelet derived growth factors (PDGF), insulin-likegrowth factors (IGF), fibroblast growth factors (FGF), epidermal growthfactor (EGF), human endothelial cell growth factor (ECGF), granulocytemacrophage colony stimulating factor (GM-CSF), vascular endothelialgrowth factor (VEGF), cartilage derived morphogenetic protein (CDMP),other bone morphogenetic proteins such as OP-1, OP-2, BMP3, BMP4, BMP9,BMP11, BMP14, DPP, Vg-1, 60A, and Vgr-1, collagens, elastic fibers,reticular fibers, glycoproteins or glycosaminoglycans, such as heparinsulfate, chondroitin-4-sulfate, chondroitin-6-sulfate, dermatan sulfate,keratin sulfate, etc. For example, growth factors such as TGF-13, withascorbate, have been found to trigger chondrocyte differentiation andcartilage formation by chondrocytes. In addition, hyaluronic acid is agood substrate for the attachment of chondrocytes and other stromalcells and can be incorporated as part of the scaffold or coated onto thescaffold.

Additionally, other factors which influence the growth and/or activityof particular cells may also be used. For example, in the case ofchondrocytes, a factor such as a chondroitinase which stimulatescartilage production by chondrocytes can be added to the matrix in orderto maintain chondrocytes in a hypertrophic state as described in U.S.Patent Application No. 2002/0122790 incorporated herein by reference. Inanother aspect, the methods of the present invention include thepresence of polysulphated alginates or other polysulphatedpolysaccharides such as polysulphated cyclodextrin and/or polysulphatedinulin, or other components capable of stimulating production of ECM ofconnective tissue cells as described in International Patent PublicationNo. WO 2005/054446 incorporated herein by reference.

The cell or tissue to be repaired and/or regenerated may be contacted invivo or in vitro by any of the methods described herein. For example,the ECM compositions may be injected or implanted (e.g., via ECM tissue,a patch or coated device of the present invention) into the subject. Inanother aspect, the tissue or cells to be repaired and/or regeneratedmay be harvested from the subject and cultured in vitro and subsequentlyimplanted or administered to the subject using known surgicaltechniques.

As discussed above, the ECM compositions of the present invention may beprocessed in a variety of ways. Accordingly, in one embodiment, thepresent invention includes a tissue culture system. In various aspects,the culture system is composed of the ECM compositions described herein.The ECM compositions of the present invention may be incorporated intothe tissue culture system in a variety of ways. For example,compositions may be incorporated as coatings, by impregnatingthree-dimensional scaffold materials as described herein, or asadditives to media for culturing cells. Accordingly, in one aspect, theculture system can include three-dimensional support materialsimpregnated with any of the ECM compositions described herein, such asgrowth factors or embryonic proteins.

The ECM compositions described herein may serve as a support orthree-dimensional support for the growth of various cell types. Any celltype capable of cell culture is contemplated. In one aspect, the culturesystem can be used to support the growth of stem cells. In anotheraspect, the stem cells are embryonic stem cells, mesenchymal stem cellsor neuronal stem cells.

The tissue culture system may be used for generating additional ECMcompositions, such as implantable tissue. Accordingly, culturing ofcells using the tissue culture system of the present invention may beperformed in vivo or in vitro. For example, the tissue culture system ofthe present invention may be used to generate ECM compositions forinjection or implantation into a subject. The ECM compositions generatedby the tissue culture system may be processed and used in any methoddescribed herein.

The ECM compositions of the present invention may be used as abiological vehicle for cell delivery. As described herein, the ECMcompositions may include both soluble and/or non-soluble fractions. Assuch, in another embodiment of the present invention, a biologicalvehicle for cell delivery or maintenance at a site of delivery includingthe ECM compositions of the present invention, is described. The ECMcompositions of the present invention, including cells andthree-dimensional tissue compositions, may be used to promote and/orsupport growth of cells in vivo. The vehicle can be used in anyappropriate application, for example to support injections of cells,such as stem cells, into damaged heart muscle or for tendon and ligamentrepair as described above.

Appropriate cell compositions (e.g., isolated ECM cells of the presentinvention and/or additional biological agents) can be administeredbefore, after or during the ECM compositions are implanted oradministered. For example, the cells can be seeded into the site ofadministration, defect, and/or implantation before the culture system orbiological delivery vehicle is implanted into the subject.Alternatively, the appropriate cell compositions can be administeredafter (e.g., by injection into the site). The cells act therein toinduce tissue regeneration and/or cell repair. The cells can be seededby any means that allows administration of the cells to the defect site,for example, by injection. Injection of the cells can be by any meansthat maintains the viability of the cells, such as, by syringe orarthroscope.

ECM compositions have been described for promoting angiogenesis inorgans and tissues by administering such compositions to promoteendothelialization and vascularization in the heart and related tissues.Accordingly, in yet another embodiment, the present invention includes asurface coating used in association with implantation of a device in asubject including the ECM compositions described herein. The coating maybe applied to any device used in implantation or penetration of asubject, such as a pacemaker, a stent, a stent graft, a vascularprosthesis, a heart valve, a shunt, a drug delivery port or a catheter.In certain aspects, the coating can be used for modifying wound healing,modifying inflammation, modifying a fibrous capsule formation, modifyingtissue ingrowth, or modifying cell ingrowth. In another embodiment, thepresent invention includes a for treatment of damaged tissue, such asheart, intestinal, infarcted or ischemic tissue. Presented below areexamples discussing generation of ECM compositions contemplated for suchapplications. The preparation and use of ECM compositions grown undernormal oxygen conditions is described in U.S. Patent Application No.2004/0219134 incorporated herein by reference.

In another embodiment, the present invention includes variousimplantable devices and tissue regeneration patches including the ECMcompositions described herein which allow for benefits, such as tissueingrowth. As discussed herein, the ECM compositions may serve ascoatings on medical devices, such as patches or other implantabledevices. In various aspects, such devices are useful for wound repair,hernia repair, pelvic floor repair (e.g., pelvic organ prolapse),rotator cuff repair and the like. In related aspects, coatings areuseful for orthopedic implants, cardiovascular implants, urinary slingsand pacemaker slings.

For example, the basic manifestation of a hernia is a protrusion of theabdominal contents into a defect within the fascia. Surgical approachestoward hernia repair is focused on reducing the hernial contents intothe peritoneal cavity and producing a firm closure of the fascial defecteither by using prosthetic, allogeneic or autogenous materials. A numberof techniques have been used to produce this closure, however, drawbacksto current products and procedures include hernia recurrence, where theclosure weakens again, allowing the abdominal contents back into thedefect. In herniorrhaphy, a corrective tissue regeneration patch, suchas a bioresorbable or synthetic mesh coated with ECM compositions couldbe used.

A variety of techniques are known in the art for applying biologicalcoatings to medical device surfaces that may be utilized with thepresent invention. For example, ECM compositions may be coated usingphotoactive crosslinkers allowing for permanent covalent bonding todevice surfaces upon activation of the crosslinker by applyingultraviolet radiation. An exemplary crosslinker is TriLite™ crosslinker,which has been shown to be non-cytotoxic, non-irritating to biologicaltissue and non-sensitizing. ECM materials may be unseparated orseparated into individual components, such as human collagens,hyaluronic acid (HA), fibronectin, and the like before coating orincorporation into various implantable devices. Further, additionalgrowth factors and such may be incorporated to allow for beneficialimplantation characteristics, such as improved cell infiltration.

In various related embodiments, the present invention provides methodsand devices applicable in cosmetic/cosmeceutical applications, such as,but not limited to anti-aging, anti-wrinkle, skin fillers, moisturizers,pigmentation augmentation, skin firming, and the like. Accordingly, inone embodiment the present invention includes a method for improvementof a skin surface in a subject including administering to the subject atthe site of a wrinkle, the ECM compositions described herein. In arelated embodiment, the present invention includes a method for softtissue repair or augmentation in a subject including administering tothe subject at the site of a wrinkle, the ECM compositions describedherein. In various cosmetic applications, the compositions may beformulated as appropriate, such as injectable and topical formulations.As discussed further in the Examples included herein, ECM compositionsformulated as topicals have been shown to be effective in various skinaesthetics applications, such as anti-wrinkle, anti-aging applicationsas well as an adjunct to ablative laser surgery. Several beneficialcharacteristics of ECM containing topicals have been shown. Suchbenefits include 1) facilitating re-epithelization followingresurfacing; 2) reduction of non-ablative and ablative fractional laserresurfacing symptoms (e.g., erythema, edema, crusting, and sensorialdiscomfort); 3) generating smooth, even textured skin; 4) generatingskin moisturization; 5) reducing appearance of fine lines/wrinkles; 6)increasing skin firmness and suppleness; 7) reducing skindyspigmentation; and 8) reducing red, blotchy skin.

The compositions of the present invention may be prepared as known inthe art, however employing the innovative culture methods describedherein (e.g., culture under hypoxic conditions). The preparation and useof ECM compositions created under normal oxygen culture conditions forthe repair and/or regeneration of cells, improvement of skin surfaces,and soft tissue repair are described in U.S. Pat. No. 5,830,708, U.S.Pat. No. 6,284,284, U.S. Patent Application No. 2002/0019339 and U.S.Patent Application No. 2002/0038152 incorporated herein by reference.

In another embodiment, the present invention includes a biologicalanti-adhesion agent including the ECM compositions described herein. Theagent can be used in such applications as anti-adhesion patches usedafter the creation of intestinal or blood vessel anastomises.

The compositions or active components used herein, will generally beused in an amount effective to treat or prevent the particular diseasebeing treated. The compositions may be administered therapeutically toachieve therapeutic benefit or prophylactically to achieve prophylacticbenefit. By therapeutic benefit is meant eradication or amelioration ofthe underlying condition or disorder being treated. Therapeutic benefitalso includes halting or slowing the progression of the disease,regardless of whether improvement is realized.

The amount of the composition administered will depend upon a variety offactors, including, for example, the type of composition, the particularindication being treated, the mode of administration, whether thedesired benefit is prophylactic or therapeutic, the severity of theindication being treated and the age and weight of the patient, andeffectiveness of the dosage form. Determination of an effective dosageis well within the capabilities of those skilled in the art.

Initial dosages may be estimated initially from in vitro assays. Initialdosages can also be estimated from in vivo data, such as animal models.Animals models useful for testing the efficacy of compositions forenhancing hair growth include, among others, rodents, primates, andother mammals. The skilled artisans can determine dosages suitable forhuman administration by extrapolation from the in vitro and animal data.

Dosage amounts will depend upon, among other factors, the activity ofthe conditioned media, the mode of administration, the condition beingtreated, and various factors discussed above. Dosage amount and intervalmay be adjusted individually to provide levels sufficient to themaintain the therapeutic or prophylactic effect.

Presented below are examples discussing generation of ECM compositionscontemplated for the discussed applications. The following examples areprovided to further illustrate the embodiments of the present invention,but are not intended to limit the scope of the invention. While they aretypical of those that might be used, other procedures, methodologies, ortechniques known to those skilled in the art may alternatively be used.

Example 1 Differential Gene Expression in ECM Compositions Grown UnderHypoxic Conditions

Primary human neonatal foreskin fibroblasts were cultured as standardmonolayers in tissue culture flasks and compared to three-dimensionalfibroblast cultures, within a naturally deposited, fetal-like ECM. Thecultures were grown as disclosed herein. To assess differentialexpression of genes, samples of total RNA were completed using AgilentWhole Human Genome Oligo Microarrays® for global gene expression(including less than 40,000 genes) following the manufacturer'sprotocol.

Upon comparison, fibroblasts were found to regulate collagen and ECMgene expression in three-dimensional cultures within a hypoxic culturednaturally secreted ECM. Upregulation and downregulation of expression ofvarious collagen and ECM genes are evident in Table 3.

TABLE 3 Differential Collagen and ECM Expression in HypoxicThree-dimensional Fibroblast Cultures GENE FOLD INCREASE FOLD DECREASECOL4A1 17.2 COL20A1 6.88 COL19A1 5.22 COL9A1 4.81 COL10A1 4.45 COL6A33.48 COL9A2 2.48 COL14A1 2 SPARC 2.74 COL1A2 3.45 COL13A1 4 COL18A1 4.76COL1A2 7.14

Upon comparison, fibroblasts were found to regulate gene expression ofWnt pathway genes in three-dimensional cultures within a hypoxiccultured naturally secreted ECM. Upregulation and downregulation ofexpression of various Wnt pathway genes are evident in Table 4.

TABLE 4 Differential Wnt Expression in Hypoxic Three-dimensionalFibroblast Cultures GENE FOLD INCREASE FOLD DECREASE WNT4 5.94 WNT7a5.43 WNT7b 4.05 WNT2b 3.95 WNT10a 3.86 WNT8b 3.48 WNT6 3.36 WNT3a 3.19WNT9b 3.06 WNT9a 3.02 WNT11 2.89 WNT5a 8.33 WNT2 7.14 WNT5b 5.26 LRP63.43 LRP3 2.27 LRP11 10 LRP12 7.69 DKK1 50 DKK3 5.88 FSZD5 4.48 FRZ93.85 FRZB 3.36 FRZD1 2.94 SFRP2 2.95 FRZD1 2.92 FRZD3 2.84 AXIN2 4.4KREMEN2 4.24 KREMEN1 3.45 b-CATENIN 4.76 GSK3b 11.1 GSK3a 6.67 bFGF 50

Upon comparison, fibroblasts were found to regulate gene expression ofbone morphogenetic protein (BMP) pathway genes in three-dimensionalcultures within a hypoxic cultured naturally secreted ECM. Upregulationand downregulation of expression of various BMP pathway genes areevident in Table 5.

TABLE 5 Differential BMP Expression in Hypoxic Three-dimensionalFibroblast Cultures GENE FOLD INCREASE FOLD DECREASE BMP7/OP1 4.88 BMP24.19 BMP5 3.49 BMP3 3.44 BMPrecIb 3.37 BMP8b 3.36 BMP8a 3.15 BMP10 2.86BMP1 2.12 BMPrecIa 2.5 Osteocalcin 2.5 Osteopontin 6.25 BMPrecII 6.25

Upon comparison, fibroblasts were found to regulate expression ofadditional genes in three-dimensional cultures within a the hypoxiccultured naturally secreted ECM. Upregulation and downregulation ofexpression of additional genes are evident in Table 6.

TABLE 6 Additional Gene Expression Changes Resulting from Low OxygenCulture of Fibroblast ECM In Vivo. FOLD FOLD GENES INCREASE DECREASECollagens COL5A1 6.21 COL9A2 3.96 COL6A2 3.78 COL6A2 3.21 COL11A1 3.07COL8A1 2.78 COL4A5 2.45 COL7A1 2.45 COL18A1 2.41 COL12A1 2.04 COL1A2 0.5COL14A1 0.45 COL4A1 0.45 COL5A2 0.23 COL6A1 0.16 MatrixMetalloproteinases (MMPs) MMP23B 2.75 MMP27 0.24 MMP28 0.17 MMP10 0.16MMP1 0.16 MMP7 0.1 MMP14 0.08 MMP3 0.06 MMP12 0.05 Other ECM HAPLN3 8.11ACAN L12234 6.48 AGC1 3.32 LAMA3 2.92 LAMA1 2.14 LAMA5 2.14

Example 2 Production of Hypoxic ECM Using Primary Human NeonatalForeskin Fibroblasts

Two examples are provided for hypoxic culture of ECM using primary humanneonatal foreskin fibroblasts.

Primary human neonatal foreskin fibroblasts were expanded in tissueculture flasks in the presence of 10% fetal bovine serum, 90% HighGlucose DMEM with 2 mM L-glutamine (10% FBS/DMEM). Cells weresubcultured using 0.05% trypsin/EDTA solution until the 3^(rd) passageat which time they were seeded to either Cytodex-1 dextran beads at 0.04mgs dry beads/ml of medium (5e⁶ cells/10 mgs beads in a 125 ml spinnerflask filled with 100-120 mis), or to nylon mesh (25e⁶ cells/6×100 cm²nylon). All cultures were kept in normal atmosphere and 5% CO₂ forexpansion and seeding, at which point low oxygen cultures were split toan airtight chamber which was flooded with 95% nitrogen/5% CO₂ so that ahypoxic environment could be created within the culture medium. Thissystem is maintains about 1-5% oxygen within the culture vessel. Cellswere mixed well into the minimum volume needed to cover nylon or beadsfor seeding, and were subsequently mixed once after 30 minutes, thenallowed to sit overnight in a humidified 37° C. incubator. Cultures werefed 10% FBS/DMEM for 2-4 weeks with a 50-70% media exchange, every 2-3days while cells proliferated and then began depositing ECM. Cultureswere fed for another 4-6 weeks using 10% bovine calf serum with ironsupplement, and 20 ug/ml ascorbic acid in place of FBS. Spinner flaskswere mixed at 15-25 rpm initially and for about 2-4 weeks, at which timethey were increased to 45 rpm and maintained at this rate thereafter.Bead cultures formed large amorphous structures containing ECM of asmuch as 0.5 to 1.0 cm in width and diameter after 4 weeks, and thesecultures were therefore hypoxic due to gas diffusion and high metabolicrequirements.

In an additional example, primary human neonatal foreskin fibroblastswere expanded in monolayer flasks, and then cultured on nylon meshscaffolds to support development of an ECM in vitro. Fibroblasts wereexpanded in DMEM with high glucose, 2 mM L-glutamine, and 10% (v/v)fetal bovine serum. Cultures were also supplemented with 20 μg/mlascorbic acid. After 3 weeks in ambient oxygen (approximately 16%-20%oxygen) duplicate ECM-containing cultures were switched to hypoxicculture conditions (1%-5% oxygen) in a sealed chamber flushedextensively with 95% nitrogen/5% carbon dioxide (Cat.#MC-101,Billups-Rothenberg, Inc., Del Mar, Calif.). To ensure depletion ofatmospheric oxygen from the culture medium, 2-3 hours later theatmosphere was replaced to ensure that the medium containedapproximately 1-3% oxygen. Both sets of ECM-containing cultures weregrown with twice weekly feedings for another 4 weeks, and then cultureswere prepared for RNA isolation. Total cellular RNA was isolated using acommercially available kit according to he manufacturers instructions(Cat.# Z3100, Promega, Inc.). Purified RNA samples were stored at −80°C., prior to processing for microarray analysis of gene expression usingAgilent Whole Human Genome Oligo Microarrays®.

In analyzing the results, there were approximately 5,500 differentiallyexpressed transcripts detected from probes prepared from ambient oxygenin comparison to probes from low oxygen cultures, using Agilent WholeHuman Genome Oligo Microarrays®. Of these, about half (2,500) weregreater than 2.0 fold increased by low oxygen, and about half (2,500)were decreased greater than 2.0 fold in low oxygen. This indicates thatlow oxygen led to significant changes in gene expression in vitro. Ofparticular interest, transcripts for ECM proteins, particularly a numberof collagen genes were up-regulated, while a number of genes formatrix-degrading enzymes were down-regulated.

Example 3 Tissue-Engineered Human Embryonic Extracellular Matrix forTherapeutic Applications

The embryonic ECM creates an environment conducive to rapid cellproliferation and healing without the formation of scars or adhesions.It was hypothesized that the growth of human neonatal fibroblasts in 3dimensions under conditions that simulate the early embryonicenvironment prior to angiogenesis (hypoxia and reduced gravitationalforces) would generate an ECM with fetal properties. Gene chip arrayanalysis showed the differential expression of over 5000 genes under thehypoxic versus traditional tissue culture conditions. The ECM producedwas similar to fetal mesenchymal tissue in that it is relatively rich incollagens type III, IV, and V, and glycoproteins such as fibronectin,SPARC, thrombospondin, and hyaluronic acid. Since the ECM also plays animportant regulatory role in binding and presenting growth factors inputative niches which support regenerative stem cell populations withkey growth factors, we evaluated the effects of hypoxia on growth factorexpression during the development of the fetal-like ECM in culture.Hypoxia can also enhance expression of factors which regulate woundhealing and organogenesis, such as VEGF, FGF-7, and TGF-β, as well asmultiple wnts including wnts 2b, 4, 7a, 10a, and 11. The embryonic humanECM also stimulated an increase of metabolic activity in humanfibroblasts in vitro, as measured by increased enzymatic activity usingthe MTT assay. Additionally, we detected an increase in cell number inresponse to human ECM. This human ECM can be used as a biologicalsurface coating, and tissue filler treatment in various therapeuticapplications where new tissue growth and healing without scarring oradhesions.

Example 4 Production of Naturally-Soluble WNT Activity for RegenerativeMedicine Applications

Stem or progenitor cells that can regenerate adult tissues, such as skinor blood, recapitulate embryonic development to some extent toaccomplish this regeneration. A growing number of studies have shownthat key regulators of stem cell pluripotency and lineage-specificdifferentiation active during embryogenesis are re-expressed in theadult under certain circumstances. The WNT family of secretedmorphogenetic growth and development factors is among the growth factorswhich can potentially provide valuable research tools and eventuallytherapeutic treatments in the clinic. However, Wnt's have provenrefractory to standard recombinant expression and purificationtechniques to date on a commercial scale, and there are no reports oflarge-scale WNT protein production to enable clinical development ofWNT-based products. Techniques have been developed for growingfetal-like ECM in culture using neonatal human dermal fibroblasts onvarious scaffolds in culture to generate three-dimensionaltissue-equivalents. In this process, it was discovered that thesecultures can provide a commercial-scale source of bioactive WNT'scontained in the serum-free conditioned medium used for ECM production.Here we present data on this WNT product candidate.

Gene expression analysis of the cells demonstrated that at least 3 WNTgenes were expressed (wnt 5a, wnt 7a, and wnt 11), and a small number ofgenes related to wnt signaling were expressed as well; however, theirfunction is not completely understood. The gene expression data wasextended to an in vitro bioassay for wnt-signaling (nucleartranslocation of β-catenin in primary human epidermal keratinocytes) andwnt activity on blood stem cells was evaluated. Both assays demonstratedactivity consistent with canonical wnt activity. Furthermore,conditioned media from these cultures showed wnt activity when injectedinto the skin of mice, inducing hair follicle stem cells to enteranagen, thus causing hair growth. This indicates that the stabilized WNTactivity within the defined and serum-free condition medium did notrequire purification. This product can be used for hair follicleregeneration and as a valuable research tool for the culture of varioushuman stem cells.

Example 5 Hypdxic Fibroblasts Demonstrate Unique ECM Production andGrowth Factor Expression

Human neonatal dermal fibroblasts produce an ECM when cultured in vitro,which closely mimics the dermis and which can replace the damaged dermisin regenerative medicine applications such as wound healing. Since theprocess of wound healing also recapitulates embryonic development, bysimulating the embryonic environment we hypothesize that the ECMproduced will provide an enhanced ECM for tissue regenerationapplications. Therefore, human neonatal fibroblast-derived ECM weregrown under hypoxic conditions in culture, to simulate the hypoxia whichexists in the early embryo prior to angiogenesis. The goal was togenerate an ECM with fetal properties using hypoxic conditions duringtissue development in culture.

The ECM produced in these hypoxic cultures was similar to fetalmesenchymal tissue in that it is relatively rich in collagens type IIIand V, and glycoproteins such as fibronectin, SPARC, thrombospondin, andhyaluronic acid. Since the ECM also plays an important regulatory rolein binding and presenting growth factors in putative niches whichsupport regenerative stem cell populations with key growth factors, weevaluated the effects of hypoxia on growth factor expression during thedevelopment of the fetal-like ECM in culture. It was shown that hypoxiacan also enhance expression of factors which regulate wound healing andorganogenesis, such as VEGF, FGF-7, and TGF-β.

The human ECM also stimulated an increase of metabolic activity in humanfibroblasts in vitro, as measured by increased enzymatic activity usingthe MTT assay. Additionally, an increase in cell number in response tohuman ECM was detected. These results support the use of this human ECMas a coating/scaffold in embryonic cell cultures and as a biologicalsurface coating/filler in various therapeutic applications or medicaldevices.

Example 6 Human Extracellular Matrix (hECM) Coated Biomedical Materials

ECM compositions generated using human derived materials (hECM) werecoated onto propylene mesh using a photoactive crosslinker.Anti-fibronectin immunofluorescent stains of hECM-coated polypropylenemesh show that the ECM materials form a uniform coating on the fibers ofthe mesh as compared to uncoated mesh. HECM coated mesh is suitable forimplantable patches for medical applications, such as hernia repair andpelvic floor repair. The ECM materials are shown to coat the individualfibers of the mesh as shown through immunofluorescent staining withfibronectin antibodies which allows for improved cellular ingrowth.

Biocompatibility evaluations were performed at 2 weeks and 5 weeks afterimplantation of hECM coated polypropylene mesh. The number offoreign-body giant cells (FBGCs) were examined. The number of FBGCs perfiber 2 weeks after implantation is shown in FIGS. 1A-B. The number offoreign-body giant cells per fiber 5 weeks after implantation is shownin FIGS. 2A-B. A reduction in FBGCs for hECM coated polypropylene meshas compared with non-coated mesh is evident.

A mechanism of FBGC formation is the result of macrophage fusion in animmune response to implantable biomaterials such as polypropylene. Theselarge multinucleated cells provide an effective means to quantitativelyassess the inflammatory response to implantable biomaterials. Asignificant reduction in FBGC count per sample with human ECM coatedversus uncoated polypropylene was observed at the two week time point.This data suggests that the human ECM surface coating may serve as anapplication for a variety of implantable devices.

Historically, the effectiveness and longevity of implantable deviceshave been challenged by specific immune responses including FBGC andfibrous capsule formation. Specifically FBGCs can excrete degradativeagents such as superoxides and free radicals. These negative effects areespecially significant since FBGCs are known to remain localizedimmediately around the implant for the duration of the presence of theimplant. Fibrous capsule formation, which arises as a firm vascularcollagen encapsulation around an implant, is designed to isolate foreignimplantables from the host or host tissue. This response not only maycause discomfort for the patient in certain cases, but may shortenlength of device viability and even diminish device effectiveness. Thusa coating that reduces FBGC and fibrous encapsulation is a highlydesirable outcome for the longevity and function of implantable devices.

Example 7 Use of Extracellular Matrix Compositions for Stimulation ofHair Growth

This example illustrates the stimulation of hair growth byadministration of ECM compositions.

Human hair follicle cells and cells taken from hair follicles wereobtained to determine the ability of the ECM compositions describedherein to stimulate and maintain hair forming ability. Hair folliclecells were obtained from Alderans Research International. Cells werecultivated in the presence of ECM. Analysis of the cells at four weeksand eight weeks of culture showed structures that resembled hairfollicles as well as structures that resembled hair shafts as shown inFIGS. 3A and B. After two months of continuous culture, the cellsremained alive and growing.

Cells cultured for four weeks in the presence of ECM composition weretransplanted into mice. Four weeks after transplantation the culturedhuman hair follicles formed many large follicles as compared to controlcells which showed only normal numbers of small resting hair folliclesas observed using microscopic image analysis.

Example 8 Generation of Human Extracellular Matrix Compositions (heCM)

Human ECM composition was generated using newborn human fibroblasts.Fibroblasts were seeded onto beadlike structures conditioned with liquidmedia. Culture conditions were optimized without the need for fetalbovine serum. Within a few days, under embryonic culture conditionsdescribed herein, cells produced a dense embryonic like ECM. Secretionof Wnt family proteins, as well as several growth factors was observed.

Cultures were grown to confluency. The cultures were subsequentlyexposed to sterile water to induce uniform lysing of the cells. Theacellular hECM was then washed to ensure removal of all living cells andcellular debris and examined microscopically to confirm removal ofcellular debris. Next, human fibroblasts were exposed to culture flaskscoated with the hECM or plated onto a non-treated flask and then coveredwith a thick layer of matrix. The ECM proteins identified in the hECMare shown in Table 7.

TABLE 7 Extracellular Matrix Proteins Observed in hECM Matrix ProteinFunction Versican structural, binds hyaluronic acid (HA) and collagenDecorin binds growth factors, influences collagen structure BetaglycanTGF-β Type III receptor Syndecan binds growth factors, enhances activityCollagen Type major structural proteins of dermis I, II, III, VFibronectin cell adhesion, spreading, migration, motogenesis Tenascininduced in wound healing, control of cell adhesion

The hECM was observed to induce an increase of metabolic activity of thecells, as measured by increased enzymatic activity using the MTT assayas shown in FIG. 4. Human ECM, unlike mouse ECM, induced adose-dependant increase in cellular metabilic activity as measured byMTT assay. Cells were observed to rapidly and uniformly infiltrate thehECM overlay material. In addition, there was a dose-dependant increasein cell number in response to hECM, as measured by the Pico Green assayas shown in FIG. 5.

Known coatings, injectables, and implantable matrix products aretypically either bovine collagens, porcine matrix proteins derived fromthe intestines or urinary bladder, hyaluronic acid, or human ECM derivedfrom cadaver skin. While these products may offer benefits by creating amore physiologically equivalent environment, none are completely humanand contain the entire range of matrix proteins found in young,developing tissue. The hECM produced contains the same ECM materialsfound in young, healthy tissue. It also was observed to support theactive proliferation of human cells as well as rapid in-growth of cells.There are several advantages evident in using hECM in applicationsinvolving a human subject. For example, hECM promotes rapid host cellintegration and improved healing (acts as normal scaffold for host cellsand subsequent remodeling). Additionally, hECM eliminates the concernregarding viral transmission from non-human animal and human tissues(particularly BSE from bovine tissue and TSE from human tissue).Further, consistent product composition and performance is observed forhECM as compared to biologic products, particularly human dermis andfascia lata. Additionally, hECM reduces erosion of host tissues ascompared to synthetic implants.

Example 9 Human Fibroblast Derived Hypoxic Conditioned ExtracellularMatrix for Medical Aesthetic Applications

A double blind, randomized study of topical hECM administration postfacial ablative laser surgery was conducted. The study enrolled 41subjects between the ages of 40 and 60 years of age. All members of thestudy group were without prior invasive or minimally invasive surgery,or topical anti-aging treatments within the prior 12 months. The laserprocedure included full fractional ablative laser procedure,peri-ocular, peri-oral and full face. A Palomar Starluz 550p laser wasused (1540-non-ablative and 2940 ablative). Subjects were administeredtopical hECM compositions once a day (at different concentrations) orplacebo vehicle for 14 days. End points of the study included clinicalphotography (3 blinded evaluations-dermatologists), transepidermal waterloss (TEWL), punch biopsy, and evaluation of erythema, edema, andcrusting.

The 10× strength hECM composition provided the most clinical improvementin symptoms as compared to the vehicle control (evaluations wereconducted “blindly” by two cosmetic dermatologists, unrelated to anyconduct of the clinical study). The results are shown in FIGS. 6(erythema), 7 (edema), and 8 (crusting). Photographic evaluation alsoindicated a reduction of erythema severity in several patients at days3, 7 and 14.

Transepidermal water loss (TEWL) values were also evaluated 3, 7, and 14days post laser treatment for all 41 subjects. The results are shown inFIG. 9. The 10× strength hECM composition provided improvement instratum corneum barrier function as noted at day 3, and day 7 ascompared to the vehicle control. At day 7, the hECM composition isstatistically significant at (p<0.05) as compared to the vehiclecontrol. This observation is consistent with the fact that there weresubjects at day 7 post ablative fractional laser treatment that weredemonstrating reepithelialization.

A double blind, randomized study of topical hECM administration foranti-aging (e.g., wrinkle reduction) was also conducted. The studyenrolled 26 subjects between the ages of 40 and 65 years of age. Allmembers of the study group were without prior invasive or minimallyinvasive surgery, or topical anti-aging treatments within the prior 12months. Subjects were administered topical hECM compositions twice a dayor placebo vehicle for 10 weeks. Endpoints of the study includedclinical photography (2 blinded cosmetic dermatologists),corneometer-surface hydration, cutometer-elasticity, punch biopsy,molecular evaluation (Epidermal Genetic Information Retrieval (EGIR)).

Photographic evaluation of the facial area indicated a generation oflighter pigmentation, smoother skin texture, more evenly toned skin, anda reduction in the appearance of fine wrinkles and lines after 10 weeksof hECM administration.

Three dimensional profilometry image analysis of silicon replicas of theperi-ocular area was also performed for 22 of the 26 subjects. Toperform the analysis a collimated light source was directed at a 25°angle from the plane of the replica. The replica was placed in a holderthat fixed the direction of the tab position of the replica so that thereplica could be rotated to align the tab direction normal or parallelto the incident light direction. The replicas were taken from the crow'sfeet area adjacent to each eye with the tab direction pointing towardthe ear. The normal sampling orientation provided texture measurementssensitive to the major, expression-induced lines (crow's feet). Theparallel sampling orientation provided texture measurements sensitive tothe minor, fine lines. The results are shown in FIG. 10.

A double blind, randomized study of topical hECM administration postfacial ablative laser surgery was conducted. The study enrolled 49subjects between the ages of 40 and 60 years of age. All members of thestudy group were without prior invasive or minimally invasive surgery,or topical anti-aging treatments within the prior 12 months. The laserprocedure included full fractional ablative laser procedure,peri-ocular, peri-oral and full face. A Palomar Starluz 550p laser wasused (1540-non-ablative and 2940 ablative). Subjects were administeredtopical hECM compositions twice a day or placebo vehicle for 14 days.End points of the study included clinical photography (3 blindedevaluations-dermatologists), mexameter and subject assessment.

Photographic evaluation of the facial area at days 1, 3, 5, 7 and 14post surgery showed a clear reduction in erythema at every time point ascompared to placebo.

Days of petrolatum use was assessed post surgery as shown in FIG. 11.Erythema grading was conducted as shown in FIG. 12. Mexameter resultsare shown in FIG. 13 for both ablative (2940) and non-ablative (1540)laser settings.

The results of the studies indicated several beneficial characteristicsof hECM containing topicals. Such benefits included 1) facilitatingre-epithelization following resurfacing; 2) reduction of non-ablativeand ablative fractional laser resurfacing symptoms (e.g., erythema,edema, crusting, and sensorial discomfort); 3) generating smooth, eventextured skin; 4) generating skin moisturization; 5) reducing appearanceof fine lines/wrinkles; 6) increasing skin firmness and suppleness; 7)reducing skin dyspigmentation; and 8) reducing red, blotchy skin.

Although the invention has been described with reference to the aboveexamples, it will be understood that modifications and variations areencompassed within the spirit and scope of the invention. Accordingly,the invention is limited only by the following claims.

1. A method of making a composition comprising one or more embryonicproteins comprising: culturing cells under hypoxic conditions on asurface in a suitable growth medium, thereby producing a soluble and anon-soluble composition comprising one or more embryonic proteins. 2.The method of claim 1, wherein the growth medium comprises serum.
 3. Themethod of claim 1, wherein the growth medium is serum-free.
 4. Themethod of claim 1, wherein the hypoxic oxygen conditions are 1-5%oxygen.
 5. The method of claim 1, wherein collagen species areupregulated as compared with media produced in oxygen conditions ofabout 15-20% oxygen.
 6. The method of claim 5, wherein the collagen isselected from type V alpha 1; IX alpha 1; IX alpha 2; VI alpha 2; VIIIalpha 1; IV, alpha 5; VII alpha 1; XVIII alpha 1; or XII alpha
 1. 7. Themethod of claim 1, wherein Wnt species are upregulated as compared withmedia produced in oxygen conditions of about 15-20% oxygen.
 8. Themethod of claim 7, wherein the Wnt species are wnt 7a and wnt
 11. 9. Themethod of claim 1, wherein laminin species are upregulated as comparedwith media produced in oxygen conditions of about 15-20% oxygen.
 10. Themethod of claim 9, wherein the laminin species is laminin
 8. 11. Themethod of claim 1, wherein the cell-free supernatant is dialyzed,lyophilized and reconstituted in a buffer.
 12. The method of claim 1,wherein the cell-free supernatant is dialyzed, desiccated andreconstituted in a buffer.
 13. The method of claim 1, wherein the cellsare fibroblasts.
 14. The method of claim 13, wherein the fibroblasts areneonatal fibroblasts.
 15. The method of claim 1, wherein the surface isthree-dimensional.
 16. The method of claim 15, wherein the surfacecomprises mesh.
 17. The method of claim 1, wherein the surface istwo-dimensional.
 18. The method of claim 17, wherein the surfacecomprises beads.
 19. The method of claim 1, wherein the cells arespecies specific.
 20. A composition prepared by the method of claim 1,wherein the composition is the soluble fraction.
 21. A compositionprepared by the method of claim 1, wherein the composition is thenon-soluble fraction.
 22. A composition prepared by the method of claim1, wherein the composition is a combination of the soluble andnon-soluble fraction.
 23. A method of repair and/or regeneration ofcells comprising contacting cells to be repaired or regenerated with thecomposition of any of claim 20, 21 or
 22. 24. The method of claim 23,wherein the cells are osteochondral cells.
 25. A tissue regenerationpatch comprising a composition of any of claim 20, 21 or
 22. 26. Atissue culture system including a composition as in any of claim 20, 21or
 22. 27. The tissue culture system of claim 26, wherein the system isused to support the growth of stem cells.
 28. The tissue culture systemof claim 27, wherein the stem cells are embryonic stem cells,mesenchymal stem cells or neuronal stem cells.
 29. A surface coatingused in association with implantation of a device in a subjectcomprising a composition of any of claim 20, 21 or
 22. 30. The coatingof claim 29, wherein the device is a pacemaker, a stent, a stent graft,a vascular prosthesis, a heart valve, a shunt, a drug delivery port, acatheter, or a patch.
 31. The coating of claim 29, wherein the coatingis used for modifying wound healing, modifying inflammation, modifying afibrous capsule formation, modifying tissue ingrowth, or modifying cellingrowth.
 32. A method of treating damaged tissue comprising contactingthe damaged tissue with a composition as in any of claim 20, 21 or 22under conditions that allow for treatment of the damaged tissue.
 33. Themethod of claim 32, wherein the tissue is heart tissue.
 34. The methodof claim 32, wherein the tissue is infarcted or ischemic tissue.
 35. Themethod of claim 32, wherein the tissue is intestinal tissue.
 36. Amethod for improvement of a skin surface in a subject comprisingadministering to the subject at the site of a wrinkle, a composition asin any of claim 20, 21 or 22, thereby providing an improved skinsurface.
 37. A biological anti-adhesion agent comprising a compositionas in any of claim 20, 21 or
 22. 38. A biological vehicle for celldelivery or maintenance at a site of delivery comprising a compositionas in any of claim 20, 21 or
 22. 39. A method for soft tissue repair oraugmentation in a subject comprising administering to the subject at thesite of a wrinkle, a composition as in any of claim 20, 21 or 22,thereby providing soft tissue repair or augmentation.
 40. A method ofpromoting hair growth comprising contacting a cell with a composition asin any of claim 20, 21 or 22, thereby promoting hair growth.
 41. Amethod of claim 40, wherein the cell is a hair follicle cell.
 42. Themethod of claim 40, wherein the cell is contacted in vivo.
 43. Themethod of claim 40, wherein the cell is contacted ex vivo.
 44. Themethod of claim 43, wherein the cell is transplanted into a subject. 45.A method of producing a Wnt protein and a vascular endothelial growthfactor (VEGF) comprising: culturing cells under hypoxic conditions on asurface in a suitable growth medium, thereby producing the Wnt proteinand the VEGF.
 46. The method of claim 45, wherein the growth medium isserum-free.
 47. The method of claim 45, wherein the hypoxic oxygenconditions are 1-5% oxygen.
 48. The method of claim 47, wherein Wntspecies are upregulated as compared with media produced in oxygenconditions of about 15-20% oxygen.
 49. The method of claim 48, whereinthe Wnt species are wnt 7a and wnt
 11. 50. The method of claim 45,wherein VEGF species are upregulated as compared with media produced inoxygen conditions of about 15-20% oxygen.
 51. The method of claim 50,wherein the VEGF species is VEGF-A or isoform thereof.
 52. The method ofclaim 45, wherein the cells are fibroblasts.
 53. The method of claim 45,wherein the surface is three-dimensional.
 54. The method of claim 53,wherein the surface comprises mesh.
 55. The method of claim 45, whereinthe surface is two-dimensional.
 56. The method of claim 55, wherein thesurface comprises beads.